Viral vectors for the treatment of retinal dystrophy

ABSTRACT

The present invention relates to viral vectors that are capable of delivering a heterologous gene to the retina and in particular delivering RLBP1 to RPE and Müller cells of the retina. The invention also relates nucleic acids useful for producing viral vectors, compositions comprising the viral vectors and uses of the compositions and viral vectors. The invention also relates to methods of delivering and/or expressing a heterologous gene to the retina, improving the rate of dark adaption in a subject and treating RLBP1-associated retinal dystrophy.

RELATED APPLICATIONS

This application claims priority to U.S. Provisional Application No. 61/642,630 filed May 4, 2012 and U.S. Provisional Application No. 61/776,167 filed Mar. 11, 2013, the contents of which are incorporated herein by reference in their entireties.

SEQUENCE LISTING

The instant application contains a Sequence Listing which has been submitted in ASCII format via EFS-Web and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Aug. 16, 2013 is named PAT055109-US-NP_SL.txt and is 253,289 bytes in size.

BACKGROUND OF THE INVENTION

Retinitis pigmentosa (RP) refers to a group of inherited degenerations of the photoreceptor cells (rods and cones) of the retina leading to visual loss and blindness. Mutations in any of a wide variety of genes can cause RP, including genes encoding proteins that are involved in phototransduction (the process by which the energy of a photon of light is converted in the photoreceptor cell outer segment into a neuronal signal), the visual cycle (production and recycling of vitamin A in the retina), photoreceptor structure, and transcription factors (Phelan and Bok, 2000).

RLBP1-associated retinal dystrophy is a rare form of RP caused by mutations in the retinaldehyde binding protein 1 (RLBP1) gene on chromosome 15. Mutations in this gene cause absence of or dysfunction of cellular retinaldehyde-binding protein (CRALBP), a protein that is important in the visual cycle (He et al 2009). CRALBP is expressed in retinal pigment epithelium (RPE) and Müller cells, ciliary epithelium, iris, cornea, pineal gland and a subset of oligodendrocytes of the optic nerve and brain (Saari et al 1997). CRALBP accepts 11-cis-retinol from the isomerase RPE65 and acts as a carrier of this substrate for 11-cis-retinol dehydrogenase (RDH5) to convert the substrate into 11-cis-retinal. The rate of chromophore regeneration is severely reduced in the absence of functional CRALBP (Travis et al 2007). The function of CRALBP outside the RPE is not well understood, but it has been suggested that CRALBP in the Müller cells supports a cone-specific visual pathway that permits cone cells to quickly adapt to a wide range of light intensities (Wang and Kefalov 2011).

RLBP1-associated retinal dystrophy is characterized by early severe night blindness and slow dark adaptation, followed by progressive loss of visual acuity, visual fields and color vision leading to legal blindness typically around middle adulthood. The fundus appearance is characterized by yellow or white spots in the retina. The reduction in visual acuity and visual field significantly impacts patients' quality of life (Burstedt and Mönestam, 2010).

The most common RLBP1 mutations leading to RLBP1-associated retinal dystrophy are recessive mutations, designated R234W and M226K (Golovleva I and Burstedt M 2012). RLBP1-associated retinal dystrophy caused by 1 or both of these recessive missense mutations is also known as Bothnia Dystrophy. Several other loss-of-function mutations in the RLBP1 gene have been reported to lead to RLBP1-associated retinal dystrophy. For example, splice-junction mutations in RLBP1 cause rod-cone dystrophy in Newfoundland. Currently there is no treatment available for RLBP1-associated retinal dystrophy (Eichers et al 2002).

The present invention is based in part on the discovery that expression of RLBP1 from recombinant adeno-associated viral vectors (rAAV) having a combination of selected promoter, AAV genome and capsid serotype provides a potent and efficacious treatment for RLBP1-associated retinal dystrophy.

SUMMARY OF THE INVENTION

The present invention relates generally to recombinant viral vectors and methods of using recombinant viral vectors to express proteins in the retina of subjects suffering from retinal diseases and blindness.

The present invention relates to viral vectors that are capable of delivering a heterologous gene to the retina. The present invention also relates to viral vectors that are capable of directing a heterologous gene to RPE and Müller cells of the retina. The present invention further relates to viral vectors that are recombinant adeno-associated viral vectors (rAAV). In certain embodiments the rAAV viral vector may be selected from among any AAV serotype known in the art, including, without limitation, AAV1-AAV12. In certain embodiments, the rAAV vector capsid is an AAV2 serotype. In certain other embodiments, the rAAV vector capsid is an AAV8 serotype.

The invention relates, in part, to viral vectors carrying a single stranded vector genome. In the single stranded viral vector, the vector genome can include a 5′ ITR, a recombinant nucleotide sequence comprising an RLBP1 coding sequence, and a 3′ ITR. The recombinant nucleic acid sequence of the vector genome can also include a promoter as described herein. In one aspect, the promoter is an RLBP1 (long) promoter (SEQ ID NO: 10), in another aspect the promoter is an RLBP1 (short) promoter (SEQ ID NO: 3). In certain specific aspects of the invention, the vector genome comprises, in the 5′ to 3′ direction, nucleic acid sequences selected from: a) SEQ ID NO: 2, 10, 5, 6, 8, and 9; b) SEQ ID NO: 2, 11, 5, 6, 8, 14, 9; c) SEQ ID NO: 2, 22, 5, 6, 8, 23, and 9; and d) SEQ ID NO: 2, 3, 4, 5, 6, 8, 23, and 9.

The invention also relates, in part, to viral vectors carrying a self-complementary genome. The self-complementary vector genome can include, from 5′ to 3′, a 5′ ITR, a first recombinant nucleotide sequence, a non-resolvable ITR (e.g.: ΔITR), a second recombinant nucleotide sequence, and a 3′ ITR, wherein the first and second recombinant nucleotide sequences are self-complementary. The second recombinant nucleotide sequence comprises in the 5′ to 3′ direction, a promoter, an RLBP1 coding sequence and an SV40 polyA sequence. The promoter can be an RLBP1 promoter and, further, can be the RLBP1 (short) promoter (SEQ ID NO: 3). In certain aspects of the invention, the second recombinant nucleotide sequence comprises nucleic acid sequences in the 5′ to 3′ direction of SEQ ID NO: 3, 4, 5, 6, and 8 and the first recombinant nucleotide sequence comprises sequences that are self-complementary to, or the reverse complement of, the second recombinant sequence, for example, SEQ ID NOs: 62, 63, 64, 65, and 66. The invention also relates to a viral vector comprising a self-complementary vector genome wherein the genome comprises, nucleic acid sequences in the 5′ to 3′ direction of: SEQ ID NOs: 36, 62, 63, 64, 65, 66, 1, 3, 4, 5, 6, 8, and 9. The self-complementary vector genome described above can be packaged in an AAV capsid that is selected from any AAV serotype known in the art, including but not limited to AAV1-12. In one aspect, the self-complementary genome is packaged in an AAV8 capsid. In another aspect, the self-complementary genome is packaged in an AAV2 capsid.

The present invention also relates to a viral vector capable of directing expression of a heterologous gene to RPE and Müller cells of the retina. It is contemplated that the viral vector capsid is an AAV2 or an AAV8 serotype capsid and that the viral vector comprises a vector genome, wherein the heterologous gene is operably linked to an RLBP1 promoter. It is further contemplated that the RLBP1 promoter is the RLBP1 (short) promoter (SEQ ID NO: 3) or the RLBP1 (long) promoter (SEQ ID NO: 10). In another aspect of the invention it is contemplated that the heterologous gene to be expressed in RPE and Müller cells is an RLBP1 coding sequence having for example, the sequence of SEQ ID NO: 6.

The present invention also relates to a viral vector capable of directing expression of a heterologous gene to RPE and Müller cells of the retina, wherein the viral vector capsid is an AAV8 serotype capsid and that the viral vector comprises a self-complementary vector genome wherein a heterologous gene is operably linked to an RLBP1 promoter. It is further contemplated that the RLBP1 promoter is the RLBP1 (short) promoter (SEQ ID NO: 3). In another aspect of the invention it is contemplated that the heterologous gene to be expressed in RPE and Müller cells is an RLBP1 coding sequence having for example, the sequence of SEQ ID NO: 6.

The invention also relates to a composition comprising a viral vector described herein, as well as viral vector compositions in combination with a pharmaceutically acceptable carrier. Specifically, the invention further relates to compositions comprising the viral vectors as described in Table 4. The invention still further relates to compositions comprising viral vectors that can be generated using the plasmids described in Table 2, in conjunction with rAAV production methods known in the art and described herein. The compositions described herein are useful for treating a subject having RLBP1 associated retinal dystrophy and/or improving the rate of dark adaption in a subject having RLBP1-associated retinal dystrophy.

The present invention also relates to nucleic acids that can be used, with the rAAV production methods known in the art and described herein, for the generation of the viral vectors described herein. The invention relates to nucleic acids comprising a gene cassette, wherein the gene cassette comprises, in the 5′ to 3′ direction: (i) a 5′ ITR or a non-resolvable ITR, (ii) a recombinant nucleotide sequence comprising an RLBP1 coding sequence, and (iii) a 3′ ITR. It is contemplated that the nucleic acid may comprise a gene cassette comprising a nucleic acid sequence selected from SEQ ID NOs: 51, 52, 53, 54, and 55. It is contemplated that the nucleic acids of the invention may be plasmids. It is further contemplated that the nucleic acid may be a plasmid comprising a nucleic acid sequence selected from SEQ ID NOs: 26, 27, 28, 29, 30 and 50.

In certain specific aspects of the invention, the nucleic acid can comprise a gene cassette comprising sequences in the 5′ to 3′ direction that are selected from: a) a) SEQ ID NO: 2, 10, 5, 6, 8, and 9, b) SEQ ID NO: 2, 11, 5, 6, 8, 14 and 9, c) SEQ ID NO: 2, 22, 5, 6, 8, 23 and 9, d) SEQ ID NO: 2, 3, 4, 5, 6, 8, 23 and 9, or e) SEQ ID NO: 1, 3, 4, 5, 6, 8, and 9.

The invention also relates to nucleic acids comprising a gene cassette, wherein the gene cassette comprises, in the 5′ to 3′ direction: (i) a 5′ ITR, (ii) a recombinant nucleotide sequence comprising a promoter operably linked to reporter gene, and (iii) a 3′ ITR. It is contemplated that the nucleic acid may comprise a gene cassette comprising a nucleic acid sequence selected from SEQ ID NOs: 56, 57, 59 and 60. It is further contemplated that nucleic acid may be a plasmid comprising a nucleic acid sequence selected from SEQ ID NOs: 31, 32, 34 and 35.

The invention also relates to methods of treating a subject having RLBP1-associated retinal dystrophy wherein the method comprises administering to a subject in need thereof, a composition comprising a viral vector as described herein.

The invention also relates to a method of improving the rate of dark adaption in a subject having RLBP1-associated retinal dystrophy, wherein the method comprises administering to a subject in need thereof, a composition comprising a viral vector as described herein.

The invention still further relates to a method of directing expression of an RLBP1 coding sequence in RPE and Müller cells in the retina of a subject having RLBP1-associated retinal dystrophy, wherein the method comprises the step of contacting the retina of the subject, with a viral vector comprising an AAV8 or AAV2 serotype capsid and a vector genome comprising an RLBP1 coding sequence operably linked to an RLBP1 promoter, such as, for example, the RLBP1(short) (SEQ ID NO: 3) or RLBP1(long) (SEQ ID NO: 10) promoters as described herein.

The invention still further relates to a method of delivering an RLBP1 coding sequence in RPE and Müller cells in the retina of a subject having RLBP1-associated retinal dystrophy, wherein the method comprises the step of contacting the retina of the subject, with a viral vector comprising an AAV8 or AAV2 serotype capsid and a vector genome comprising an RLBP1 coding sequence operably linked to an RLBP1 promoter, such as, for example, the RLBP1(short) (SEQ ID NO: 3) or RLBP1(long) (SEQ ID NO: 10) promoters as described herein.

The invention also includes a viral vector as described in Table 1, or 4, as well as a plasmid described in Table 2.

DEFINITIONS

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by those of ordinary skill in the art to which this invention pertains.

The term “capsid” refers to the protein coat of the virus or viral vector. The term “AAV capsid” refers to the protein coat of the adeno-associated virus (AAV), which is composed of a total of 60 subunits; each subunit is an amino acid sequence, which can be viral protein 1(VP1), VP2 or VP3 (Muzyczka N and Berns K I 2001).

The term “gene cassette” refers to a manipulatable fragment of DNA carrying, and capable of expressing, one or more genes, or coding sequences, of interest between one or more sets of restriction sites. A gene cassette can be transferred from one DNA sequence (often in a plasmid vector) to another by ‘cutting’ the fragment out using restriction enzymes and ligating it back into a new context, for example into a new plasmid backbone.

The term “heterologous gene” or “heterologous nucleotide sequence” will typically refer to a gene or nucleotide sequence that is not naturally-occurring in the virus. Alternatively, a heterologous gene or nucleotide sequence may refer to a viral sequence that is placed into a non-naturally occurring environment (e.g.: by association with a promoter with which it is not naturally associated in the virus).

The terms “ITR” or “inverted terminal repeat” refer to the stretch of nucleic acid sequences that exist in Adeno-Associated Viruses (AAV) and/or recombinant Adeno-Associated Viral Vectors (rAAV) that can form a T-shaped palindromic structure, that is required for completing AAV lytic and latent life cycles (Muzyczka N and Berns K I 2001). The term “non-resolvable ITR” refers to a modified ITR such that the resolution by the Rep protein is reduced. A non-resolvable ITR can be an ITR sequence without the terminal resolution site (TRS) which leads to low or no resolution of the non-resolvable ITR and would yield 90-95% of self-complementary AAV vectors (McCarty et al 2003). A specific example of a non-resolvable ITR is “ΔITR”, having a sequence of SEQ ID NO: 1.

The term “operably linked” refers to a functional relationship between two or more polynucleotide (e.g., DNA) segments. Typically, the term refers to the functional relationship of a transcriptional regulatory sequence to a sequence to be transcribed. For example, a promoter or enhancer sequence is operably linked to a coding sequence if it stimulates or modulates the transcription of the coding sequence in an appropriate host cell or other expression system. Generally, promoter transcriptional regulatory sequences that are operably linked to a transcribable sequence are contiguous to the transcribable sequence, i.e., they are cis-acting. However, some transcriptional regulatory sequences, such as enhancers, need not be physically contiguous or located in close proximity to the coding sequences whose transcription they enhance.

The term “promoter” refers to a sequence that regulates transcription of an operably-linked gene, or nucleotide sequence encoding a protein, etc. Promoters provide the sequence sufficient to direct transcription, as well as, the recognition sites for RNA polymerase and other transcription factors required for efficient transcription and can direct cell specific expression. In addition to the sequence sufficient to direct transcription, a promoter sequence of the invention can also include sequences of other regulatory elements that are involved in modulating transcription (e.g.: enhancers, kozak sequences and introns). Examples of promoters known in the art and useful in the viral vectors described herein, include the CMV promoter, CBA promoter, smCBA promoter and those promoters derived from an immunoglobulin gene, SV40, or other tissue specific genes (e.g: RLBP1, RPE, VMD2). Specific promoters may also include those described in Table 1, for example, the “RLBP1 (short)” promoter (SEQ ID NO: 3), the “RLBP1 (long)” promoter (SEQ ID NO: 10), RPE65 promoter (SEQ ID NO: 11), VMD2 promoter (SEQ ID NO: 12), and the CMV enhancer+CBA promoter (SEQ ID NO: 22). In addition, standard techniques are known in the art for creating functional promoters by mixing and matching known regulatory elements. “Truncated promoters” may also be generated from promoter fragments or by mix and matching fragments of known regulatory elements; for example the smCBA promoter is a truncated form of the CBA promoter.

The term “RLBP1” refers to the “Retinaldehyde Binding Protein 1”. The human RLBP1 gene is found on chromosome 15 and has the nucleic acid coding sequence as set out in Table 1: SEQ ID NO: 6. The “RLBP1 gene product” is also known as, “cellular retinaldehyde binding protein” or “CRALBP” and is the protein encoded by the RLBP1 gene. The human RLBP1 gene product (hCRALBP) has the amino acid sequence as set out in Table 1: SEQ ID NO: 7. Examples of RLBP1 coding sequences and RLBP1 gene products from other species can be found in Table 1 (e.g.: SEQ ID NOs: 37-48). The term “RLBP1 coding sequence” or “RLBP1 GENE CDS” or “RLBP1 CDS” refers to the nucleic acid sequence that encodes the RLBP1 gene product. One of skill in the art would understand that an RLBP1 coding sequence may include any nucleic acid sequence that encodes an RLBP1 gene product. The RLBP1 coding sequence may or may not include intervening regulatory elements (e.g.: introns, enhancers, or other non-coding sequences).

The term “subject” includes human and non-human animals. Non-human animals include all vertebrates (e.g.: mammals and non-mammals) such as, non-human primates (e.g.: cynomolgus monkey), mice, rats, sheep, dogs, cows, chickens, amphibians, and reptiles. Except when noted, the terms “patient” or “subject” are used herein interchangeably.

As used herein, the term “treating” or “treatment” of any disease or disorder (e.g., retinitis pigmentosa, RBLP1-associated retinal dystrophy) refers, to ameliorating the disease or disorder such as by slowing or arresting or reducing the development of the disease or at least one of the clinical symptoms thereof. “Treating” or “treatment” can also refer to alleviating or ameliorating at least one physical parameter including those which may not be discernible by the patient. “Treating” or “treatment” can also refer to modulating the disease or disorder, either physically, (e.g., stabilization of a discernible symptom), physiologically, (e.g., stabilization of a physical parameter), or both. More specifically, “treatment” of RLBP1-associated retinal dystrophy means any action that results in the improvement or preservation of visual function and/or regional anatomy in a subject having RLBP1-associated retinal dystrophy. “Preventing or “prevention” as used herein, refers to preventing or delaying the onset or development or progression of the disease or disorder. “Prevention” as it relates to RLBP1-associated retinal dystrophy means any action that prevents or slows a worsening in visual function, retinal anatomy, and/or an RLBP1-associated retinal dystrophy disease parameter, as described below, in a patient with RLBP1-associated retinal dystrophy and at risk for said worsening. Methods for assessing treatment and/or prevention of disease are known in the art and described herein below.

The term “virus vector” or “viral vector” is intended to refer to a non-wild-type recombinant viral particle (e.g.: a parvovirus, etc.) that functions as a gene delivery vehicle and which comprises a recombinant viral genome packaged within a viral (e.g.: AAV) capsid. A specific type of virus vector may be a “recombinant adeno-associated virus vector”, or “rAAV vector”. The recombinant viral genome packaged in the a viral vector is also referred to herein as the “vector genome”.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. Relative expression of vector-mediated human RLBP1 mRNA compared to endogenous mouse RLBP1 mRNA in eyes injected with various viral vectors at the dosage of 1×10⁹ (1A) and 1×10⁸ (1B) vector genome (vg) particles per eye.

FIG. 2. Dark adaptation in RLBP1 KO (−/−) and wild-type (+/+) mice.

FIG. 3. Measurement of rate of dark adaptation of RLBP1 KO mice treated with various viral vectors: NVS1 (3B), NVS3 (3A and 3C), NVS3 (3B and 3D), NVS4 (3A and 3C) and NVS5 (3B and 3D).

FIG. 4. Measurement of increased rate of dark adaptation of RLBP1 KO mice treated with various doses of NVS2 and NVS11 is shown in panel 4A. Panel 4B illustrates treatment efficacy of NVS2. Horizontal axis doses are indicated in scientific notation (for example, 3E6=3×10⁶).

FIG. 5. Measurement of increased rate of dark adaptation of RLBP1 KO mice treated with various doses of NVS4 and NVS11 is shown in panel 5A. Panel 5B illustrates treatment efficacy of NVS4. Horizontal axis doses are indicated in scientific notation (for example, 3E6=3×10⁶).

FIG. 6. Measurement of increased rate of dark adaptation of RLBP1 KO mice treated with NVS2 prepared with different purification methods.

DETAILED DESCRIPTION

The present invention is based, in part, on the discovery of viral vectors that express a heterologous gene in RPE and Müller cells of the retina. The invention also relates both to single stranded and self-complementary viral vectors with a heterologous gene expressing the RLBP1 gene product (CRALBP).

Accordingly, the present invention provides recombinant viral vectors that direct expression of the RLBP1 coding sequence to the retina, viral vector compositions, plasmids useful for generating the viral vectors, methods of delivering an RLBP1 coding sequence to the retina, methods of expressing an RLBP1 coding sequence in RPE and Müller cells of the retina, and methods of use of such viral vectors.

Except as otherwise indicated, standard methods known to those skilled in the art may be used for the construction of recombinant parvovirus and rAAV vectors, using recombinant plasmids carrying a viral gene cassette, packaging plasmids expressing the parvovirus rep and/or cap sequences, as well as transiently and stably transfected packaging cells. Such techniques are known to those skilled in the art. (e.g.: SAMBROOK et al., MOLECULAR CLONING: A LABORATORY MANUAL 2nd Ed. (Cold Spring Harbor, N.Y., 1989); Choi V W et al. CURRENT PROTOCOLS IN MOLECULAR BIOLOGY (2007)).

1. Viral Vectors

The present invention is related to viral vectors that direct expression of a heterologous gene to the retina. In certain aspects of the invention, expression is directed to RPE and Müller cells of the retina. A variety of viral vectors known in the art may be adapted by one of skill in the art for use in the present invention, for example, recombinant adeno-associated viruses, recombinant adenoviruses, recombinant retroviruses, recombinant poxviruses, recombinant baculoviruses, etc.

In particular, it is contemplated that the viral vector of the invention may be a recombinant adeno-associated (rAAV) vector. AAVs are small, single-stranded DNA viruses which require helper virus to facilitate efficient replication (Muzyczka N and Berns K I 2001). The viral vector comprises a vector genome and a protein capsid. The viral vector capsid may be supplied from any of the AAV serotypes known in the art, including presently identified human and non-human AAV serotypes and AAV serotypes yet to be identified (See: Choi V W et al 2005, Schmidt et al 2008). Virus capsids may be mixed and matched with other vector components to form a hybrid viral vector, for example the ITRs and capsid of the viral vector may come from different AAV serotypes. In one aspect, the ITRs can be from an AAV2 serotype while the capsid is from, for example, an AAV2 or AAV8 serotype. In addition, one of skill in the art would recognize that the vector capsid may also be a mosaic capsid (e.g.: a capsid composed of a mixture of capsid proteins from different serotypes), or even a chimeric capsid (e.g.: a capsid protein containing a foreign or unrelated protein sequence for generating markers and/or altering tissue tropism). It is contemplated that the viral vector of the invention may comprise an AAV2 capsid. It is further contemplated that the invention may comprise an AAV8 capsid.

The invention relates, in part, to viral vectors wherein the vector genome is single stranded. In certain aspects, the invention is related to a single stranded vector genome comprising, in the 5′ to 3′ direction: (i) a 5′ ITR, (ii) a recombinant nucleotide sequence comprising an RLBP1 coding sequence, and (iii) a 3′ ITR. In certain aspects of the invention the recombinant nucleotide sequence comprises in the 5′ to 3′ direction: (i) a promoter, (ii) an RLBP1 coding sequence, and (iii) an SV40 polyA sequence. In certain aspects, the promoter may be an RLBP1 (short) promoter, an RLBP1 (long) promoter, or a truncated promoter of RLBP1. In particular, the invention relates to a single stranded vector genome comprising a recombinant nucleotide sequence comprising in the 5′ to 3′ direction: an RLBP1 (long) promoter (SEQ ID NO:10), an RLBP1 coding sequence, and an SV40 polyA sequence. In addition, the invention also relates to a single stranded vector genome comprising a recombinant nucleotide sequence comprising in the 5′ to 3′ direction: an RLBP1 (short) promoter (SEQ ID NO: 3), an RLBP1 coding sequence, and an SV40 polyA sequence. Certain aspects of the invention further relate to a single stranded vector genome comprising a recombinant nucleotide sequence packaged in an AAV2 or AAV8 capsid.

In certain aspects of the invention the viral vector comprises an AAV2 capsid (encoded by SEQ ID NO: 18) and a vector genome comprising in the 5′ to 3 direction nucleotide sequences selected from the following: a) SEQ ID NO: 2, 10, 5, 6, 8, and 9; b) SEQ ID NO: 2, 11, 5, 6, 8, 14, 9; c) SEQ ID NO: 2, 22, 5, 6, 8, 23, and 9; and d) SEQ ID NO: 2, 3, 4, 5, 6, 8, 23, and 9. In certain aspects the AAV2 capsid comprises capsid proteins VP1, VP2 and VP3 having an amino acid sequence of SEQ ID NO: 19, 68, and 69, respectively. In certain other aspects the AAV2 capsid may comprise subcombinations of capsid proteins VP1, VP2 and/or VP3.

In certain aspects of the invention the viral vector comprises an AAV8 capsid (encoded by SEQ ID NO: 20) and a vector genome comprising in the 5′ to 3′ direction nucleotide sequences selected from the following: a) SEQ ID NO: 2, 10, 5, 6, 8, and 9; b) SEQ ID NO: 2, 11, 5, 6, 8, 14, 9; c) SEQ ID NO: 2, 22, 5, 6, 8, 23, and 9; and d) SEQ ID NO: 2, 3, 4, 5, 6, 8, 23, and 9. In certain aspects the AAV8 capsid comprises capsid proteins VP1, VP2 and VP3 having an amino acid sequence of SEQ ID NO: 21, 70, and 71. In certain other aspects the AAV8 capsid may comprise subcombinations of capsid proteins VP1, VP2 and/or VP3.

The viral vector can also be an AAV vector comprising a self-complementary genome. Self-complementary rAAV vectors have been previously described in the art (U.S. Pat. No. 7,465,583 and McCarty 2008) and may be adapted for use in the present invention. A self-complementary genome comprises a 5′ ITR and a 3′ ITR (i.e.: resolvable ITR or wild-type ITR) at either end of the genome and a non-resolvable ITR (e.g.: ΔITR, as described herein) interposed between the 5′ and 3′ ITRs. Each portion of the genome (i.e. between each resolvable ITR and non-resolvable ITR) comprises a recombinant nucleotide sequence, wherein each half (i.e.: the first recombinant nucleotide sequence and the second recombinant nucleotide sequence) is complementary to the other, or self-complementary. In other words, the self-complementary vector genome is essentially an inverted repeat with the two halves joined by the non-resolvable ITR. In certain aspects the invention is related to a self-complementary vector genome comprising, in the 5′ to 3′ direction, (i) a 5′ ITR, (ii) a first recombinant nucleotide sequence, (iii) a non-resolvable ITR, (iv) a second recombinant nucleotide sequence, and (v) a 3′ ITR. In a certain aspect of the invention the second recombinant nucleotide sequence of the vector genome comprises, an RLBP1 promoter, an RLBP1 coding sequence, and an SV40 polyA sequence and the first recombinant nucleotide sequence is self-complementary to the second nucleotide sequence. In certain specific aspects the RLBP1 promoter has the nucleotide sequence of SEQ ID NO: 3. In certain aspects of the invention, the second recombinant nucleotide sequence comprises nucleic acid sequences in the 5′ to 3′ direction of SEQ ID NO: 3, 4, 5, 6, and 8 and the first recombinant nucleotide sequence comprises sequences that are self-complementary to, or the reverse complement of, the second recombinant sequence, for example, SEQ ID NOs: 62, 63, 64, 65, and 66. It is also contemplated that the viral vector of the invention may comprise a self-complementary genome wherein the first recombinant nucleotide sequence of the vector genome comprises, an RLBP1 promoter, an RLBP1 coding sequence, and an SV40 polyA sequence and the second recombinant nucleotide sequence is self-complementary to the first recombinant nucleotide sequence.

In certain aspects of the invention the self-complementary viral vector comprises an AAV2 capsid (encoded by SEQ ID NO: 18) and a vector genome comprising a nucleotide sequence comprising sequences in the 5′ to 3′ direction SEQ ID NO: 36, SEQ ID NO: 62, SEQ ID NO: 63, SEQ ID NO: 64, SEQ ID NO: 65, SEQ ID NO: 66, SEQ ID NO: 1, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 8, and SEQ ID NO: 9. In certain aspects the AAV2 capsid comprises capsid proteins VP1, VP2 and VP3 having an amino acid sequence of SEQ ID NO: 19, 68, and 69, respectively. In certain other aspects the AAV2 capsid may comprise subcombinations of capsid proteins VP1, VP2 and/or VP3.

In certain aspects of the invention the self-complementary viral vector comprises an AAV8 capsid (encoded by SEQ ID NO: 20) and a vector genome comprising a nucleotide sequence comprising sequences in the 5′ to 3′ direction SEQ ID NO: 36, SEQ ID NO: 62, SEQ ID NO: 63, SEQ ID NO: 64, SEQ ID NO: 65, SEQ ID NO: 66, SEQ ID NO: 1, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 8, and SEQ ID NO: 9. In certain aspects the AAV8 capsid comprises capsid proteins VP1, VP2 and VP3 having an amino acid sequence of SEQ ID NO: 21, 70, and 71. In certain other aspects the AAV8 capsid may comprise subcombinations of capsid proteins VP1, VP2 and/or VP3.

Thus, the invention also relates to viral vectors as described herein, comprising a truncated promoter of RLBP1.

The invention further relates to a viral vector that directs expression of a heterologous gene to RPE and Müller cells of the retina, wherein the viral vector comprises an AAV8 capsid and a vector genome comprising an RLBP1 (short) promoter (SEQ ID NO:3) operably linked to a heterologous gene. In certain aspects of the invention, the vector genome is a self-complementary genome.

The invention also relates to methods of expressing RLBP1 in RPE cells and Müller cells of the retina. In certain aspects of the invention the method comprises contacting the retinal cells with a viral vector comprising an AAV capsid and a vector genome comprising an RLBP1 coding sequence operably linked to an RLBP1 promoter, which may be an RLBP1 (short) promoter (SEQ ID NO:3). In certain aspects of the invention the AAV capsid is AAV2. In certain other aspects, the AAV capsid is AAV8. In other aspects of the invention the method comprises contacting the retinal cells with a viral vector comprising an AAV capsid and a vector genome comprising an RLBP1 coding sequence operably linked to an RLBP1 promoter, which may be an RLBP1 (long) promoter (SEQ ID NO: 10). In certain aspects of the invention the AAV capsid is AAV2. In certain other aspects, the AAV capsid is AAV8.

Methods for generating viral vectors are well known in the art and would allow for the skilled artisan to generate the viral vectors of the invention (see, e.g., U.S. Pat. No. 7,465,583), including the viral vectors described in Table 4, using the plasmids described in Table 2 and the Examples.

In general, methods of producing rAAV vectors are applicable to producing the viral vectors of the invention; the primary difference between the methods is the structure of the genetic elements to be packaged. To produce a viral vector according to the present invention, sequences of the genetic elements and plasmids as described in table 2 can be used to produce the encapsidated viral genome.

The genetic elements as described in table 2 are in the context of a circular plasmid, but one of skill in the art will appreciated that a DNA substrate may be provided in any form known in the art, including but not limited to a plasmid, naked DNA vector, bacterial artificial chromosome (BAC), yeast artificial chromosome (YAC) or a viral vector (e.g., adenovirus, herpesvirus, Epstein-Barr Virus, AAV, baculoviral, retroviral vectors, and the like). Alternatively, the genetic elements in table 2 necessary to produce the viral vectors described herein may be stably incorporated into the genome of a packaging cell.

The viral vector particles according to the invention may be produced by any method known in the art, e.g., by introducing the sequences to be replicated and packaged into a permissive or packaging cell, as those terms are understood in the art (e.g., a “permissive” cell can be infected or transduced by the virus; a “packaging” cell is a stably transformed cell providing helper functions).

In one embodiment, a method is provided for producing an RLBP1 viral vector, wherein the method comprises providing to a cell permissive for parvovirus replication: (a) a nucleotide sequence containing the genetic elements for producing a vector genome of the invention (as described in detail below and in table 2); (b) nucleotide sequences sufficient for replication of the vector genome sequence in (a) to produce a vector genome; (c) nucleotide sequences sufficient to package the vector genome into a parvovirus capsid, under conditions sufficient for virus vectors comprising the vector genome encapsidated within the parvovirus capsid to be produced in the cell. Preferably, the parvovirus replication and/or capsid coding sequences are AAV sequences.

Any method of introducing the nucleotide sequence carrying the gene cassettes described below into a cellular host for replication and packaging may be employed, including but not limited to, electroporation, calcium phosphate precipitation, microinjection, cationic or anionic liposomes, and liposomes in combination with a nuclear localization signal.

Viral vectors described herein may be produced using methods known in the art, such as, for example, triple transfection or baculovirus mediated virus production. Any suitable permissive or packaging cell known in the art may be employed to produce the vectors. Mammalian cells are preferred. Also preferred are trans-complementing packaging cell lines that provide functions deleted from a replication-defective helper virus, e.g., 293 cells or other E1a trans-complementing cells. Also preferred are mammalian cells or cell lines that are defective for DNA repair as known in the art, as these cell lines will be impaired in their ability to correct the mutations introduced into the plasmids described herein.

The gene cassette may contain some or all of the parvovirus (e.g., AAV) cap and rep genes. Preferably, however, some or all of the cap and rep functions are provided in trans by introducing a packaging vector(s) encoding the capsid and/or Rep proteins into the cell. Most preferably, the gene cassette does not encode the capsid or Rep proteins. Alternatively, a packaging cell line is used that is stably transformed to express the cap and/or rep genes (see, e.g., Gao et al., (1998) Human Gene Therapy 9:2353; Inoue et al., (1998) J. Virol. 72:7024; U.S. Pat. No. 5,837,484; WO 98/27207; U.S. Pat. No. 5,658,785; WO 96/17947).

In addition, helper virus functions are preferably provided for the virus vector to propagate new virus particles. Both adenovirus and herpes simplex virus may serve as helper viruses for AAV. See, e.g., BERNARD N. FIELDS et al., VIROLOGY, volume 2, chapter 69 (3d ed., Lippincott-Raven Publishers). Exemplary helper viruses include, but are not limited to, Herpes simplex (HSV) varicella zoster, cytomegalovirus, and Epstein-Barr virus. The multiplicity of infection (MOI) and the duration of the infection will depend on the type of virus used and the packaging cell line employed. Any suitable helper vector may be employed. Preferably, the helper vector is a plasmid, for example, as described by Xiao et al., (1998) J. Virology 72:2224. The vector can be introduced into the packaging cell by any suitable method known in the art, as described above.

Vector stocks free of contaminating helper virus may be obtained by any method known in the art. For example, recombinant single stranded or self complementary virus and helper virus may be readily differentiated based on size. The viruses may also be separated away from helper virus based on affinity for a heparin substrate (Zolotukhin et al. (1999) Gene Therapy 6:973). Preferably, deleted replication-defective helper viruses are used so that any contaminating helper virus is not replication competent. As a further alternative, an adenovirus helper lacking late gene expression may be employed, as only adenovirus early gene expression is required to mediate packaging of the duplexed virus. Adenovirus mutants defective for late gene expression are known in the art (e.g., ts100K and ts149 adenovirus mutants).

One method for providing helper functions employs a non-infectious adenovirus miniplasmid that carries all of the helper genes required for efficient AAV production (Ferrari et al., (1997) Nature Med. 3:1295; Xiao et al., (1998) J. Virology 72:2224). The rAAV titers obtained with adenovirus miniplasmids are forty-fold higher than those obtained with conventional methods of wild-type adenovirus infection (Xiao et al., (1998) J. Virology 72:2224). This approach obviates the need to perform co-transfections with adenovirus (Holscher et al., (1994), J. Virology 68:7169; Clark et al., (1995) Hum. Gene Ther. 6:1329; Trempe and Yang, (1993), in, Fifth Parvovirus Workshop, Crystal River, Fla.).

Other methods of producing rAAV stocks have been described, including but not limited to, methods that split the rep and cap genes onto separate expression cassettes to prevent the generation of replication-competent AAV (see, e.g., Allen et al., (1997) J. Virol. 71:6816), methods employing packaging cell lines (see, e.g., Gao et al., (1998) Human Gene Therapy 9:2353; Inoue et al., (1998) J. Virol. 72:7024; U.S. Pat. No. 5,837,484; WO 98/27207; U.S. Pat. No. 5,658,785; WO 96/17947), and other helper virus free systems (see, e.g., U.S. Pat. No. 5,945,335 to Colosi).

Herpesvirus may also be used as a helper virus in AAV packaging methods. Hybrid herpesviruses encoding the AAV Rep protein(s) may advantageously facilitate for more scalable AAV vector production schemes. A hybrid herpes simplex virus type I (HSV-1) vector expressing the AAV-2 rep and cap genes has been described (Conway et al., (1999) Gene Therapy 6:986 and WO 00/17377).

In summary, the gene cassette to be replicated and packaged, parvovirus cap genes, appropriate parvovirus rep genes, and (preferably) helper functions are provided to a cell (e.g., a permissive or packaging cell) to produce rAAV particles carrying the vector genome. The combined expression of the rep and cap genes encoded by the gene cassette and/or the packaging vector(s) and/or the stably transformed packaging cell results in the production of a viral vector particle in which a viral vector capsid packages a viral vector genome according to the invention. The single stranded or self-complementary viral vectors are allowed to assemble within the cell, and may then be recovered by any method known by those of skill in the art and described in the examples. For example, viral vectors may be purified by standard CsCl centrifugation methods (Grieger J C et al 2006) or by various methods of column chromatography known to the skilled artisan (see: Lock M et al (2010), Smith R H et al (2009) and Vadenberghe L H et al (2010)).

The reagents and methods disclosed herein may be employed to produce high-titer stocks of the inventive viral vectors, preferably at essentially wild-type titers. It is also preferred that the parvovirus stock has a titer of at least about 10⁵ transducing units (tu)/ml, more preferably at least about 10⁶ to/ml, more preferably at least about 10⁷ to/ml, yet more preferably at least about 10⁸ to/ml, yet more preferably at least about 10⁹ to/ml, still yet more preferably at least about 10¹⁰ to/ml, still more preferably at least about 10″ to/ml, or more.

Further, the RLBP1 viral vectors of the invention, may have an improved transducing unit/particle ratio over conventional AAV vectors. Preferably, the tu/particle ratio is less than about 1:50, less than about 1:20, less than about 1:15, less than about 1:10, less than about 1:8, less than about 1:7, less than about 1:6, less than about 1:5, less than about 1:4, or lower. Typically, the tu/particle ratio will be greater than about 1:1, 1:2, 1:3 or 1:4.

2. Nucleic Acids for Use in Generating the Viral Vector

The invention also relates to nucleic acids useful for the generation of viral vectors. In certain aspects of the invention, the nucleic acids useful for the generation of viral vectors may be in the form of plasmids. Plasmids useful for the generation of viral vectors, also referred to as a viral vector plasmid, may contain a gene cassette. At a minimum, a gene cassette of a viral vector plasmid contains: a heterologous gene and its regulatory elements (e.g.: promoter, enhancer, and/or introns, etc.), and 5′ and 3′ AAV inverted terminal repeats (ITRs).

The composition of the heterologous gene and its regulatory elements will depend upon the use to which the resulting vector will be put. For example, one type of heterologous gene sequence includes a reporter sequence, which upon expression produces a detectable signal. Such reporter sequences include, without limitation, DNA sequences encoding β-lactamase, β-galactosidase (LacZ), alkaline phosphatase, thymidine kinase, green fluorescent protein (GFP), chloramphenicol acetyltransferase (CAT), luciferase, membrane bound proteins including, for example, CD2, CD4, CD8, the influenza hemagglutinin protein, and others well known in the art, to which high affinity antibodies directed thereto exist or can be produced by conventional means, and fusion proteins comprising a membrane bound protein appropriately fused to an antigen tag domain from, among others, hemagglutinin or Myc. For example, where the reporter sequence is the LacZ gene, the presence of the vector carrying the signal is detected by assays for beta-galactosidase activity. Where the reporter sequence is green fluorescent protein or luciferase, the vector carrying the signal may be measured visually by color or light production in a luminometer.

The heterologous gene sequences, when associated with regulatory elements which drive their expression, provide signals detectable by conventional means, including enzymatic, radiographic, colorimetric, fluorescence or other spectrographic assays, fluorescent activating cell sorting assays and immunological assays, including enzyme linked immunosorbent assay (ELISA), radioimmunoassay (RIA) and immunohistochemistry.

The heterologous gene may also be a non-marker sequence encoding a product which is useful in biology and medicine, such as proteins, peptides, RNA, enzymes, dominant negative mutants, or catalytic RNAs. Desirable RNA molecules include tRNA, dsRNA, ribosomal RNA, catalytic RNAs, siRNA, small hairpin RNA, trans-splicing RNA, and antisense RNAs. One example of a useful RNA sequence is a sequence which inhibits or extinguishes expression of a targeted nucleic acid sequence in the treated animal.

The heterologous gene may also be used to correct or ameliorate gene deficiencies, which may include deficiencies in which normal genes are expressed at less than normal levels or deficiencies in which the functional gene product is not expressed. It is contemplated in the present invention that the heterologous gene sequence may be an RLBP1 coding sequence. Examples of RLBP1 coding sequences are provided in Table 1: SEQ ID NOs: 6, 37, 39, 41, 43, 45 or 47.

In addition to the heterologous gene, the gene cassette may include regulatory elements operably linked to the heterologous gene. These regulatory elements may include appropriate transcription initiation, termination, promoter and enhancer sequences, efficient RNA processing signals such as splicing and polyadenylation (polyA) signals; sequences that stabilize cytoplasmic mRNA; sequences that enhance translation efficiency; sequences that enhance protein stability; and when desired, sequences that enhance secretion of the encoded product. A great number of regulatory sequences, including promoters which are native, constitutive, inducible and/or tissue-specific, are known in the art and may be utilized. Regulatory element sequences of the invention include those described in Table 1, for example SEQ ID NO: 3, 4, 5, 8, 10, 11, 12 and 22.

The gene cassette may include an RLBP1 promoter with a nucleic acid sequence of SEQ ID NO: 3 or 10 operably linked to a heterologous gene. In particular, the RLBP1 short promoter (SEQ ID NO: 3) is operably linked to an RLBP1 coding sequence (SEQ ID NO: 6, 37, 39, 41, 43, 45 or 47). Alternatively, the RLBP1 long promoter (SEQ ID NO: 10) is operably linked to an RLBP1 coding sequence (SEQ ID NO: 6, 37, 39, 41, 43, 45 or 47).

It is contemplated that the ITRs of AAV serotype 2 may be used (e.g.: SEQ ID NO: 2, 9, 16, 17, 36). However, ITRs from other suitable serotypes may be selected from among any AAV serotype known in the art, as described herein. These ITRs or other AAV components may be readily isolated using techniques available to those of skill in the art from any AAV serotype known, or yet to be identified serotypes, for example, the AAV sequences may be obtained through synthetic or other suitable means by reference to published sequences such as are available in the literature or in databases such as, e.g., GenBank, PubMed, or the like. Alternatively, such AAV components may also be isolated or obtained from academic, commercial, or public sources (e.g., the American Type Culture Collection, Manassas, Va.).

It is contemplated that in certain aspects of the invention, one ITR of the gene cassette may be a modified ITR, or non-resolvable ITR, sequence without the terminal resolution site (TRS). During replication of a gene cassette comprising a non-resolvable ITR, the inability of Rep protein to resolve the non-resolvable ITRs will result in a dimeric inverted repeat sequence (i.e.: self-complementary) with a non-resolvable ITR (e.g.: ΔITR) in the middle and a wild-type ITR at each end. The resulting sequence is a self-complementary viral genome sequence such that the genome is capable of forming a hairpin structure upon release from the capsid (see also: U.S. Pat. No. 7,465,583 and McCarty (2008)) A non-resolvable ITR may be produced by any method known in the art. For example, insertion into the ITR will displace the TRS and result in a non-resolvable ITR. Preferably, the insertion is in the region of the TRS site. Alternatively, the ITR may be rendered non-resolvable by deletion of the TRS site, a specific example includes ΔITR (SEQ ID NO: 1).

The invention relates to nucleic acids that comprise a gene cassette comprising in the 5′ to 3′ direction nucleic acid sequences selected from the following: a) SEQ ID NOs: 2, 10, 5, 6, 8, and 9; b) SEQ ID NOs: 2, 11, 5, 6, 8, 14 and 9; c) SEQ ID NOs: 2, 22, 5, 6, 8, 23 and 9; d) SEQ ID NOs: 2, 3, 4, 5, 6, 8, 23 and 9; e) SEQ ID NOs: 2, 10, 5, 24, 8, and 9; f) SEQ ID NOs: 2, 11, 24, 8, 14, and 9; and g) SEQ ID NOs: 2, 12, 24, 8, 14, and 9. In certain aspects the nucleic acid comprising the gene cassette may be a plasmid. In particular, the sequence of the plasmid may have a sequence selected from SEQ ID NOs: 27, 28, 29, 30, 32, 33, 34 and 35.

The invention also relates to nucleic acids that comprise a gene cassette comprising in the 5′ to 3′ direction nucleic acid sequences selected from the following: a) SEQ ID NOs: 1, 3, 4, 5, 6, 8, and 9; and b) SEQ ID NOs: 1, 3, 4, 5, 24, 8 and 9. In certain aspects the nucleic acid comprising the gene cassette may be a plasmid. In particular, the sequence of the plasmid may have a sequence selected from SEQ ID NOs: 26, 31 and 50.

Methods for incorporating the elements in Table 2 are well known in the art and would allow for the skilled artisan to generate the nucleic acids and plasmids of the invention using the methods outlined in Table 3 and the Examples.

3 Pharmaceutical Compositions

The invention provides pharmaceutical compositions comprising the viral vectors of the invention formulated together with a pharmaceutically acceptable carrier. The compositions can additionally contain one or more other therapeutic agents that are suitable for treating or preventing, for example, RLBP1-associated retinal dystrophy, and/or retinal pigmentosa (RP). Pharmaceutically acceptable carriers enhance or stabilize the composition, or can be used to facilitate preparation of the composition. Pharmaceutically acceptable carriers include solvents, surfactants, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like that are physiologically compatible.

A pharmaceutical composition of the present invention can be administered by a variety of methods known in the art. The route and/or mode of administration vary depending upon the desired results. It is preferred that administration be subretinal. The pharmaceutically acceptable carrier should be suitable for subretinal, intravitreal, intravenous, sub-cutaneous or topical administration.

The composition should be sterile and fluid. Proper fluidity can be maintained, for example, by use of coating such as lecithin, by maintenance of required particle size in the case of dispersion and by use of surfactants. In many cases, it is preferable to include isotonic agents, for example, sugars, polyalcohols such as mannitol or sorbitol, and sodium chloride in the composition.

Pharmaceutical compositions of the invention can be prepared in accordance with methods well known and routinely practiced in the art. See, e.g., Remington: The Science and Practice of Pharmacy, Mack Publishing Co., 20th ed., 2000; and Sustained and Controlled Release Drug Delivery Systems, J. R. Robinson, ed., Marcel Dekker, Inc., New York, 1978. Pharmaceutical compositions are preferably manufactured under GMP conditions. Typically, a therapeutically effective dose or efficacious dose of the viral vector is employed in the pharmaceutical compositions of the invention. The viral vectors may be formulated into pharmaceutically acceptable dosage forms by conventional methods known to those of skill in the art. Dosage regimens are adjusted to provide the optimum desired response (e.g., a therapeutic response). For example, a single bolus may be administered, several divided doses may be administered over time or the dose may be proportionally reduced or increased as indicated by the exigencies of the therapeutic situation. It is especially advantageous to formulate parenteral compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the subjects to be treated; each unit contains a predetermined quantity of active compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier.

Actual dosage levels of the active ingredients in the pharmaceutical compositions of the present invention can be varied so as to obtain an amount of the active ingredient which is effective to achieve the desired therapeutic response for a particular patient, composition, and mode of administration, without being toxic to the patient. The selected dosage level depends upon a variety of pharmacokinetic factors including the activity of the particular compositions of the present invention employed, the route of administration, the time of administration, the rate of excretion of the particular compound being employed, the duration of the treatment, other drugs, compounds and/or materials used in combination with the particular compositions employed, the age, sex, weight, condition, general health and prior medical history of the patient being treated, and like factors.

A physician or veterinarian can start doses of the viral vectors of the invention employed in the pharmaceutical composition at levels lower than that required to achieve the desired therapeutic effect and gradually increase the dosage until the desired effect is achieved. In general, effective doses of the compositions of the present invention, for the treatment of RLBP1-associated retinal dystrophy as described herein vary depending upon many different factors, including means of administration, target site, physiological state of the patient, whether the patient is human or an animal, other medications administered, and whether treatment is prophylactic or therapeutic. Treatment dosages need to be titrated to optimize safety and efficacy. For subretinal administration with a viral vector, the dosage may range from 1×10⁸ vector genomes (vg)/eye to 1×10¹² vg/eye. For example the dosage may be, 1×10⁸ vg/eye, 2.5×10⁸ vg/eye, 5×10⁸ vg/eye, 7.5×10⁸ vg/eye, 1×10⁹ vg/eye, 2.5×10⁹ vg/eye, 5×10⁹ vg/eye, 7.5×10⁹ vg/eye, 1×10¹⁰ vg/eye, 2.5×10¹⁰ vg/eye, 5×10¹⁰ vg/eye, 7.5×10¹⁰ vg/eye, 1×10¹¹ vg/eye, 2.5×10¹¹ vg/eye, 5×10¹¹ vg/eye, 7.5×10¹¹ vg/eye, 1×10¹² vg/eye.

The viral vectors described herein are mainly used as one time doses per eye, with the possibility of repeat dosing to treat regions of the retina that are not covered in the previous dosing. The dosage of administration may vary depending on whether the treatment is prophylactic or therapeutic.

The various features and embodiments of the present invention, referred to in individual sections and embodiments above apply, as appropriate, to other sections and embodiments, mutatis mutandis. Consequently features specified in one section or embodiment may be combined with features specified in other sections or embodiments, as appropriate.

4. Therapeutic Uses

Viral vectors as described herein, can be used at a therapeutically useful concentration for the treatment of eye related diseases, by administering to a subject in need thereof, an effective amount of the viral vectors of the invention. More specifically, the present invention provides a method of treating RLBP1-associated retinal dystrophy, by administering to a subject in need thereof an effective amount of a viral vector comprising an RLBP1 coding sequence.

The present invention provides a viral vector comprising an RLBP1 coding sequence for use in treating RLBP1-associated retinal dystrophy in a subject.

Table A: RLBP1 Mutations and Associated Phenotypes of RLBP1-Associated Retinal Dystrophy.

Disease phenotypes of RLBP1-associated retinal dystrophy include: Autosomal recessive retinitis pigmentosa (AARP), Bothnia dystrophy (BD), Newfoundland rod-cone dystrophy (NFRCD), Retinitis punctata albescens (RPA) and Fundus albipunctatus (FA).

TABLE A Pigment # pts Mutation Region Disease Night Blind Yellow Dots Deposits Atrophy Reference Missense Mutations 67  R234W Sweden BD Yes Perifoveal, midperiphery In advanced Advanced Burstedt et al 2001; Golovleva et al 2010; Golovleva et al 2012 10  R234W/M226K Sweden BD Yes Perifoveal, midperiphery In advanced Advanced Köhn et al 2008; Golovleva et al 2010; Golovleva et al 2012 2 M226K Sweden BD Yes Perifoveal, midperiphery In advanced Advanced Golovleva et al 2010; Golovleva et al 2012 4 G116R Pakistan FA Yes Midperiphery No No Naz et al 2011 4 R151Q Saudi Arabia FA Yes Whole fundus No No Katsaris et al 2001 4 R151Q India ARRP Yes Whole fundus Yes Yes Maw et al 1997 1 R234W Japan BD Yes Perifoveal, midperiphery In advanced Advanced Nojima et al 2011 1 R103W R234W Japan RPA Yes Perifoveal, midperiphery In advanced Yes Nakamura et al 2011 1 G146D I201T USA RPA No Midperiphery No No Demirci et al 2004 1 R103W USA RPA Yes Midperiphery No Yes Demirci et al 2004 Truncating Mutations 26  324G_A IVS3_2T 3 C Canada NFRCD Yes Perifoveal, midperiphery No Yes Eichers et al 2002 6 R156X Pakistan FA Yes Midperiphery No No Naz et al 2011 4 R151W Gly31 (2-bp del) USA RPA Yes Midperiphery Few, peripheral No Fishman et al 2004 6 Exons 7_9 del Morocco RPA Yes Perifoveal, midperiphery No No Humbert et al 2006 Littink et al 2012 1 IVS3_2T 3 C M226K USA RPA Yes Perifoveal, midperiphery No No Morimura et al 1999 1 Q278(1-bp del) USA RPA Yes Perifoveal Few, peripheral Yes Morimura et al 1999

Use of recombinant AAV has been shown to be feasible and safe for the treatment of retinal disease (See, e.g., Bainbridge et al. 2008, Houswirth et al 2008, Maguire et al 2008). The viral vectors of the invention can be used, inter alia, to treat and prevent progression of RLBP1-associated retinal dystrophy and improve vision loss. Viral vectors of the invention can also be used in patients where other retinal dystrophy is caused by other loss of function mutations in the RLBP1 gene, for example, Autosomal recessive retinitis pigmentosa, Retinitis punctata albescens and Fundus albipunctatus.

The present invention is also relates to a method of expressing an RLBP1 coding sequence in RPE and Müller cells of the retina, by administering viral vectors of the invention to a subject in need thereof. The present invention also relates to viral vectors of the invention for use in expressing an RLBP1 coding sequence in RPE and/or Müller cells of the retina of the subject in need thereof. The invention also contemplates a method of delivering an RLBP1 coding sequence to the retina, specifically to RPE and/or Müller cells in the retina, of a subject having RLBP1-associated retinal dystrophy. It is contemplated that the an RLBP1 coding sequence is delivered to the subject in need thereof by contacting the retina,

RPE and/or Müller cells of the subject with a viral vector as described herein. Alternatively, an RLBP1 coding sequence is delivered to a subject by administering to the subject a viral vector as described herein.

The present invention further includes methods of expressing an RLBP1 coding sequence in RPE and/or Müller cells in the retina of a subject having RLBP1-associated retinal dystrophy, by contacting the retina of the subject with viral vectors of the invention. In certain aspects RPE and/or Müller cells of the retina of the subject are contacted with viral vectors of the invention.

It is further contemplated that the viral vectors used in the methods described herein comprise an AAV2 or AAV8 capsid, and the vector genome comprises an RLBP1 coding sequence operably linked to an RLBP1 promoter with a nucleotide sequence selected from SEQ ID NO: 3 or 10. It is further contemplated that the vector genome can be self-complementary.

In one aspect the viral vectors described herein can be administered subretinally or intravitreally using methods known to those of skill in the art.

Treatment and/or prevention of ocular disease such as RLBP1-associated retinal dystrophy can be determined by an ophthalmologist or health care professional using clinically relevant measurements of visual function and/or retinal anatomy. Treatment of RLBP1-associated retinal dystrophy means any action (e.g., administration of a viral vector described herein) contemplated to improve or preserve visual function and/or retinal anatomy. In addition, prevention as it relates to RLBP1-associated retinal dystrophy means any action (e.g., administration of a viral vector described herein) that prevents or slows a worsening in visual function, retinal anatomy, and/or RLBP1-associated retinal dystrophy disease phenotype, as defined herein, in a patient at risk for said worsening.

Visual function may include, for example, visual acuity, visual acuity with low illumination, visual field, central visual field, peripheral vision, contrast sensitivity, dark adaptation, photostress recovery, color discrimination, reading speed, dependence on assistive devices (e.g., large typeface, magnifying devices, telescopes), facial recognition, proficiency at operating a motor vehicle, ability to perform one or more activities of daily living, and/or patient-reported satisfaction related to visual function. Thus, treatment of retinitis pigmentosa (RP), specifically RLBP1-associated retinal dystrophy, can be said to occur where a subject has an at least 10% decrease or lack of a 10% or more increase in time to a pre-specified degree of dark adaptation. In addition, treatment of RLBP1-associated retinal dystrophy can be said to occur where a subject exhibits early severe night blindness and slow dark adaptation in young age, followed by progressive loss of visual acuity, visual fields and color vision, leading to legal blindness, determined by a qualified health care professional (i.e., ophthalmologist) (Burstedt and Mönestam, 2010).

Exemplary measures of visual function include Snellen visual acuity, ETDRS visual acuity, low-luminance visual acuity, Amsler grid, Goldmann visual field, standard automated perimetry, microperimetry, Pelli-Robson charts, SKILL card, Ishihara color plates, Farnsworth D15 or D100 color test, standard electroretinography, multifocal electroretinography, validated tests for reading speed, facial recognition, driving simulations, and patient reported satisfaction. Thus, treatment of RLBP1-associated retinal dystrophy can be said to be achieved upon a gain of or failure to lose 2 or more lines (or 10 letters) of vision on an ETDRS scale. In addition, treatment of RLBP1-associated retinal dystrophy can be said to occur where a subject exhibits at least a 10% increase or lack of 10% decrease in reading speed (words per minute). In addition, treatment of RLBP1-associated retinal dystrophy can be said to occur where a subject exhibits at least a 20% increase or lack of a 20% decrease in the proportion of correctly identified plates on an Ishihara test or correctly sequenced disks on a Farnsworth test. Thus, treatment of, for example, RLBP1-associated retinal dystrophy can be determined by, for example, improvement of rate of dark adaptation, or an improvement in, or slowing of the rate of, visual acuity loss.

Undesirable aspects of retinal anatomy that may be treated or prevented include, for example, retinal atrophy, retinal pigment epithelium atrophy, narrowing of retinal vessels, pigmentary clumping, retinal yellow/white spots, subretinal fluid.

Exemplary means of assessing retinal anatomy include fundoscopy, fundus photography, fluorescein angiography, indocyanine green angiography, optical coherence tomography (OCT), spectral domain optical coherence tomography, scanning laser ophthalmoscopy, confocal microscopy, adaptive optics, fundus autofluorescence, biopsy, necropsy, and immunohistochemistry. Thus, RLBP1-associated retinal dystrophy can be said to be treated in a subject as determined by, for example, a reduction in the rate of development of retinal atrophy.

Subjects to be treated with therapeutic agents of the present invention can also be administered other therapeutic agents or devices with known efficacy for treating retinal dystrophy such as vitamin and mineral preparations, low-vision aids, guide dogs, or other devices known to assist patients with low vision.

Currently there are no other approved therapeutic agents for the treatment of RLBP1-associated retinal dystrophy. As other new therapies emerge, the two can be administered sequentially in either order or simultaneously as clinically indicated.

EXAMPLES

The following examples are provided to further illustrate the invention but not to limit its scope. Other variants of the invention will be readily apparent to one of ordinary skill in the art and are encompassed by the appended claims.

Example 1 Construction of AAV-ITR Plasmids 1.1 Cloning of AAV-ITR Plasmids:

The nucleic acid sequences of the individual plasmid elements are described in Table 1. The sequences were either synthesized or purchased commercially. Table 2 describes the elements that exist in each plasmid that was constructed. Standard molecular biology cloning techniques were used in generating the plasmids as described in Table 3. The plasmid backbone pAAV-MCS (Stratagene®) with Ampicillin resistance or pUC57 with Kanamycin resistance was used as the backbone and starting material. The individual sequence elements were cloned in at restriction enzyme sites or using blunt end cloning.

Because the antibiotic resistance gene cassette contained in the plasmid backbone does not play a role in the production of the AAV vectors, one of skill in the art could use alternate plasmid backbones and/or antibiotic resistance gene cassettes and yield the same viral vectors. We have demonstrated that functionally equivalent NVS2 vectors can be generated using plasmids with different backbones. For example, plasmid sequences SEQ ID NO: 26 and SEQ ID NO: 50 produce functionally equivalent NVS2 vectors.

1.2. Triple Plasmid Transfection to Produce rAAV Vectors:

Recombinant AAV (rAAV) viral vectors were generated by triple transfection methods. Methods for triple transfection are known in the art (Ferrari F K et al 1997). Briefly, AAV-ITR-containing plasmids (described in Table 2), AAV-RepCap containing plasmid (carrying Rep2 and Cap2 or Cap8) and Adeno-helper plasmid (carrying genes that assist in completing AAV replication cycle) were co-transfected into 293 cells. Cells were cultured for 4 days. At the end of the culture period the cells were lysed and the vectors in the culture supernatant and in the cell lysate were purified by a standard CsCl gradient centrifugation method (method modified based on Grieger J C et al 2006). The purified viral vectors are described in Table 4.

Alternatively, GMP-like rAAV vectors were generated by the cell transfection and culture methods described above. The harvested cell culture material was then processed by column chromatography based on methods described by Lock M et al (2010), Smith R H et al (2009) and Vadenberghe L H et al (2010).

1.3. Variation of 5′ ITR Sequences:

As described previously (Samulski et al, 1983; Muzyczka et al, 1984), mutations within the terminal repeat sequences of AAV plasmids are well tolerated in generating functional AAV vectors. Even plasmids with one of the two ITRs deleted, the AAV sequences could be rescued, replicated, and infectious virions be produced, as long as the existing ITR in the construct contains the full AAV ITR sequence (Samulski et al, 1983; Muzyczka et al, 1984). Therefore, even though SEQ. ID. NO. 2 is used as the 5′ ITR sequence of all single-stranded AAV vectors described in this document, it is expected that any 5′ITR sequence that carries the terminal resolution site (i.e.: SEQ. ID. NOS. 2, 16 and 17) would produce vectors with the same functionality.

TABLE 1 Sequence of viral vector and plasmid elements AMINO ACID SEQUENCE OR POLYNUCLEOTIDE (PN) SEQUENCE ELEMENTS SEQUENCE IDENTIFIER (SEQ. ID. NO:) AND SEQUENCE ΔITR  1 cgcgctcgctcgctcactgaggccgcccgggcaaagcccgggcg tcgggcgacctttggtcgcccggcctcagtgagcgagcgagcgc gcagagagggagtgg 5′ ITR  2 ctgcgcgctcgctcgctcactgaggccgcccgggcgtcgggcga cctttggtcgcccggcctcagtgagcgagcgagcgcgcagagag ggagtggccaactccatcactaggggttcct Human RLBP1  3 Promoter(short) ttgtcctctccctgcttggccttaaccagccacatttctcaact (NT_010274.17) gaccccactcactgcagaggtgaaaactaccatgccaggtcctg ctggctgggggaggggtgggcaataggcctggatttgccagagc tgccactgtagatgtagtcatatttacgatttcccttcacctct tattaccctggtggtggtggtgggggggggggggtgctctctca gcaaccccaccccgggatcttgaggagaaagagggcagagaaaa gagggaatgggactggcccagatcccagccccacagccgggctt ccacatggccgagcaggaactccagagcaggagcacacaaagga gggctttgatgcgcctccagccaggcccaggcctctcccctctc ccctttctctctgggtcttcctttgccccactgagggcctcctg tgagcccgatttaacggaaactgtgggcggtgagaagttcctta tgacacactaatcccaacctgctgaccggaccacgcctccagcg gagggaacctctagagctccaggacattcaggtaccaggtagcc ccaaggaggagctgccga MODIFIED  4 SV40INTRON aactgaaaaaccagaaagttaactggtaagtttagtctttttgt (MODIFIED cttttatttcaggtcccggatccggtggtggtgcaaatcaaaga EF579804) actgctcctcagtggatgttgcctttacttctaggcctgtacgg aagtgttacttctgctctaaaagctgcggaattgtacccgcccc gggatcc ADDED-KOZAK  5 gccacc HUMAN RLBP1  6 GENE CDS atgtcagaaggggtgggcacgttccgcatggtacctgaagagga NM_000326.4 acaggagctccgtgcccaactggagcagctcacaaccaaggacc atggacctgtctttggcccgtgcagccagctgccccgccacacc ttgcagaaggccaaggatgagctgaacgagagagaggagacccg ggaggaggcagtgcgagagctgcaggagatggtgcaggcgcagg cggcctcgggggaggagctggcggtggccgtggcggagagggtg caagagaaggacagcggcttcttcctgcgcttcatccgcgcacg gaagttcaacgtgggccgtgcctatgagctgctcagaggctatg tgaatttccggctgcagtaccctgagctctttgacagcctgtcc ccagaggctgtccgctgcaccattgaagctggctaccctggtgt cctctctagtcgggacaagtatggccgagtggtcatgctcttca acattgagaactggcaaagtcaagaaatcacctttgatgagatc ttgcaggcatattgcttcatcctggagaagctgctggagaatga ggaaactcaaatcaatggcttctgcatcattgagaacttcaagg gctttaccatgcagcaggctgctagtctccggacttcagatctc aggaagatggtggacatgctccaggattccttcccagcccggtt caaagccatccacttcatccaccagccatggtacttcaccacga cctacaatgtggtcaagcccttcttgaagagcaagctgcttgag agggtctttgtccacggggatgacctttctggtttctaccagga gatcgatgagaacatcctgccctctgacttcgggggcacgctgc ccaagtatgatggcaaggccgttgctgagcagctctttggcccc caggcccaagctgagaacacagccttctga HUMAN RLBP1  7 GENE PRODUCT MSEGVGTFRMVPEEEQELRAQLEQLTTKDHGPVFGPCSQLPRHT (CELLULAR LQKAKDELNEREETREEAVRELQEMVQAQAASGEELAVAVAERV RETINALDEHYDE QEKDSGFFLRFIRARKFNVGRAYELLRGYVNFRLQYPELFDSLS BINDING PROTEIN - PEAVRCTIEAGYPGVLSSRDKYGRVVMLFNIENWQSQEITFDEI CRALBP) LQAYCFILEKLLENEETQINGFCIIENFKGFTMQQAASLRTSDL RKMVDMLQDSFPARFKAIHFIHQPWYFTTTYNVVKPFLKSKLLE RVFVHGDDLSGFYQEIDENILPSDFGGTLPKYDGKAVAEQLFGP QAQAENTAF SV40 POLYA  8 (EF579804) gatcataatcagccataccacatttgtagaggttttacttgctt taaaaaacctcccacacctccccctgaacctgaaacataaaatg aatgcaattgttgttgttaacttgtttattgcagcttataatgg ttacaaataaagcaatagcatcacaaatttcacaaataaagcat ttttttcactgcattctagttgtggtttgtccaaactcatcaat gtatcttatcatgtct 3′ ITR  9 (AF043303) aggaacccctagtgatggagttggccactccctctctgcgcgct cgctcgctcactgaggccgggcgaccaaaggtcgcccgacgccc gggctttgcccgggcggcctcagtgagcgagcgagcgcgcag Human RLBP1 10 Promoter(long) ttgtcctctccctgcttggccttaaccagccacatttctcaact (NT_010274.17) gaccccactcactgcagaggtgaaaactaccatgccaggtcctg ctggctgggggaggggtgggcaataggcctggatttgccagagc tgccactgtagatgtagtcatatttacgatttcccttcacctct tattaccctggtggtggtggtgggggggggggggtgctctctca gcaaccccaccccgggatcttgaggagaaagagggcagagaaaa gagggaatgggactggcccagatcccagccccacagccgggctt ccacatggccgagcaggaactccagagcaggagcacacaaagga gggctttgatgcgcctccagccaggcccaggcctctcccctctc ccctttctctctgggtcttcctttgccccactgagggcctcctg tgagcccgatttaacggaaactgtgggcggtgagaagttcctta tgacacactaatcccaacctgctgaccggaccacgcctccagcg gagggaacctctagagctccaggacattcaggtaccaggtagcc ccaaggaggagctgccgacctggcaggtaagtcaatacctgggg cttgcctgggccagggagcccaggactggggtgaggactcaggg gagcagggagaccacgtcccaagatgcctgtaaaactgaaacca cctggccattctccaggttgagccagaccaatttgatggcagat ttagcaaataaaaatacaggacacccagttaaatgtgaatttca gatgaacagcaaatacttttttagtattaaaaaagttcacattt aggctcacgcctgtaatcccagcactttgggaggccgaggcagg cagatcacctgaggtcaggagttcgagaccagcctggccaacat ggtgaaaccccatctccactaaaaataccaaaaattagccaggc gtgctggtgggcacctgtagttccagctactcaggaggctaagg caggagaattgcttgaacctgggaggcagaggttgcagtgagct gagatcgcaccattgcactctagcctgggcgacaagaacaaaac tccatctcaaaaaaaaaaaaaaaaaaaaagttcacatttaactg ggcattctgtatttaattggtaatctgagatggcagggaacagc atcagcatggtgtgagggataggcattttttcattgtgtacagc ttgtaaatcagtatttttaaaactcaaagttaatggcttgggca tatttagaaaagagttgccgcacggacttgaaccctgtattcct aaaatctaggatcttgttctgatggtctgcacaactggctgggg gtgtccagccactgtccctcttgcctgggctccccagggcagtt ctgtcagcctctccatttccattcctgttccagcaaaacccaac tgatagcacagcagcatttcagcctgtctacctctgtgcccaca tacctggatgtctaccagccagaaaggtggcttagatttggttc ctgtgggtggattatggcccccagaacttccctgtgcttgctgg gggtgtggagtggaaagagcaggaaatgggggaccctccgatac tctatgggggtcctccaagtctctttgtgcaagttagggtaata atcaatatggagctaagaaagagaaggggaactatgctttagaa caggacactgtgccaggagcattgcagaaattatatggttttca cgacagttctttttggtaggtactgttattatcctcagtttgca gatgaggaaactgagacccagaaaggttaaataacttgctaggg tcacacaagtcataactgacaaagcctgattcaaacccaggtct ccctaacctttaaggtttctatgacgccagctctcctagggagt ttgtcttcagatgtcttggctctaggtgtcaaaaaaagacttgg tgtcaggcaggcataggttcaagtcccaactctgtcacttacca actgtgactaggtgattgaactgaccatggaacctggtcacatg caggagcaggatggtgaagggttcttgaaggcacttaggcagga catttaggcaggagagaaaacctggaaacagaagagctgtctcc aaaaatacccactggggaagcaggttgtcatgtgggccatgaat gggacctgttctggtaaccaagcattgcttatgtgtccattaca tttcataacacttccatcctactttacagggaacaaccaagact ggggttaaatctcacagcctgcaagtggaagagaagaacttgaa cccaggtccaacttttgcgccacagcaggctgcctcttggtcct gacaggaagtcacaacttgggtctgagtactgatccctggctat tttttggctgtgttaccttggacaagtcacttattcctcctccc gtttcctcctatgtaaaatggaaataataatgttgaccctgggt ctgagagagtggatttgaaagtacttagtgcatcacaaagcaca gaacacacttccagtctcgtgattatgtacttatgtaactggtc atcacccatcttgagaatgaatgcattggggaaagggccatcca ctaggctgcgaagtttctgagggactccttcgggctggagaagg atggccacaggagggaggagagattgccttatcctgcagtgatc atgtcattgagaacagagccagattctttttttcctggcagggc caacttgttttaacatctaaggactgagctatttgtgtctgtgc cctttgtccaagcagtgtttcccaaagtgtagcccaagaaccat ctccctcagagccaccaggaagtgctttaaattgcaggttccta ggccacagcctgcacctgcagagtcagaatcatggaggttggga cccaggcacctgcgtttctaacaaatgcctcgggtgattctgat gcaattgaaagtttgagatccacagttctgagacaataacagaa tggtttttctaacccctgcagccctgacttcctatcctagggaa ggggccggctggagaggccaggacagagaaagcagatcccttct ttttccaaggactctgtgtcttccataggcaac HUMAN RPE65 11 PROMOTER tacgtaatatttattgaagtttaatattgtgtttgtgatacaga agtatttgctttaattctaaataaaaattttatgcttttattgc tggtttaagaagatttggattatccttgtactttgaggagaagt ttcttatttgaaatattttggaaacaggtcttttaatgtggaaa gatagatattaatctcctcttctattactctccaagatccaaca aaagtgattataccccccaaaatatgatggtagtatcttatact accatcattttataggcatagggctcttagctgcaaataatgga actaactctaataaagcagaacgcaaatattgtaaatattagag agctaacaatctctgggatggctaaaggatggagcttggaggct acccagccagtaacaatattccgggctccactgttgaatggaga cactacaactgccttggatgggcagagatattatggatgctaag ccccaggtgctaccattaggacttctaccactgtccctaacggg tggagcccatcacatgcctatgccctcactgtaaggaaatgaag ctactgttgtatatcttgggaagcacttggattaattgttatac agttttgttgaagaagacccctagggtaagtagccataactgca cactaaatttaaaattgttaatgagtttctcaaaaaaaatgtta aggttgttagctggtatagtatatatcttgcctgttttccaagg acttctttgggcagtaccttgtctgtgctggcaagcaactgaga cttaatgaaagagtattggagatatgaatgaattgatgctgtat actctcagagtgccaaacatataccaatggacaagaaggtgagg cagagagcagacaggcattagtgacaagcaaagatatgcagaat ttcattctcagcaaatcaaaagtcctcaacctggttggaagaat attggcactgaatggtatcaataaggttgctagagagggttaga ggtgcacaatgtgcttccataacattttatacttctccaatctt agcactaatcaaacatggttgaatactttgtttactataactct tacagagttataagatctgtgaagacagggacagggacaatacc catctctgtctggttcataggtggtatgtaatagatatttttaa aaataagtgagttaatgaatgagggtgagaatgaaggcacagag gtattagggggaggtgggccccagagaatggtgccaaggtccag tggggtgactgggatcagctcaggcctgacgctggccactccca cctagctcctttctttctaatctgttctcattctccttgggaag gattgaggtctctggaaaacagccaaacaactgttatgggaaca gcaagcccaaataaagccaagcatcagggggatctgagagctga aagcaacttctgttccccctccctcagctgaaggggtggggaag ggctcccaaagccataactccttttaagggatttagaaggcata aaaaggcccctggctgagaacttccttcttcattctgcagttggt HUMAN VMD2 12 PROMOTER tacgtaattctgtcattttactagggtgatgaaattcccaagca acaccatccttttcagataagggcactgaggctgagagaggagc tgaaacctacccggcgtcaccacacacaggtggcaaggctggga ccagaaaccaggactgttgactgcagcccggtattcattctttc catagcccacagggctgtcaaagaccccagggcctagtcagagg ctcctccttcctggagagttcctggcacagaagttgaagctcag cacagccccctaacccccaactctctctgcaaggcctcaggggt cagaacactggtggagcagatcctttagcctctggattttaggg ccatggtagagggggtgttgccctaaattccagccctggtctca gcccaacaccctccaagaagaaattagaggggccatggccaggc tgtgctagccgttgcttctgagcagattacaagaagggactaag acaaggactcctttgtggaggtcctggcttagggagtcaagtga cggcggctcagcactcacgtgggcagtgccagcctctaagagtg ggcaggggcactggccacagagtcccagggagtcccaccagcct agtcgccagacc SYNUCLEIN 13 INTRONIC gggccccggtgttatctcattcttttttctcctctgtaagttga SEQUENCE AS catgtgatgtgggaacaaaggggataaagtcattattttgtgct STUFFER aaaatcgtaattggagaggacctcctgttagctgggctttcttc SEQUENCE tatttattgtggtggttactggagttccttcttctagttttagg atatatatatatattttttttttttctttccctgaagatataat aatatatatacttctgaagattgagatttttaaattagttgtat tgaaaactagctaatcagcaatttaaggctagcttgagacttat gtcttgaatttgtttttgtaggctccaaaaccaaggagggagtg gtgcatggtgtggcaacaggtaagctccattgtgcttatatcca aagatgatatttaaagtatctagtgattagtgtggcccagtatt caagattcctatgaaattgtaaaacaatcactgagcattctaag aacatatcagtcttattgaaactgaattctttataaagtatttt taaaaaggtaaatattgattataaataaaaaatatacttgccaa gaataatgagggctttgaattgataagctatgtttaatttatag taagtgggcatttaaatattctgaccaaaaatgtattgacaaac tgctgacaaaaataaaatgtgaatattgccataattttaaaaaa agagtaaaatttctgttgattacagtaaaatattttgaccttaa attatgttgattacaatattcctttgataattcagagtgcattt caggaaacacccttggacagtcagtaaattgtttattgtattta tctttgtattgttatggtatagctatttgtacaaatattattgt gcaattattacatttctgattatattattcatttggcctaaatt taccaagaatttgaacaagtcaattaggtttacaatcaagaaat atcaaaaatgatgaaaaggatgataatcatcatcagatgttgag gaagatgacgatgagagtgccagaaatagagaaatcaaaggaga accaaaatttaacaaattaaaagcccacagacttgctgtaatta agttttctgttgtaagtactccacgtttcctggcagatgtggtg aagcaaaagatataatcagaaatataatttatatgatcggaaag cattaaacacaatagtgcctatacaaataaaatgttcctatcac tgacttctaaaatggaaatgaggacaatgatatgggaatcttaa tacagtgttgtggataggactaaaaacacaggagtcagatcttc ttggttcaacttcctgcttactccttaccagctgtgtgtttttt gcaaggttcttcacctctatgtgatttagcttcctcatctataa aataattcagtgaattaatgtacacaaaacatctggaaaacaaa agcaaacaatatgtattttataagtgttacttatagttttatag tgaactttcttgtgcaacatttttacaactagtggagaaaaata tttctttaaatgaatacttttgatttaaaaatcagagtgtaaaa ataaaacagactcctttgaaactagttctgttagaagttaattg tgcacctttaatgggctctgttgcaatccaacagagaagtagtt aagtaagtggactatgatggcttctagggacctcctataaatat gatattgtgaagcatgattataataagaactagataacagacag gtggagactccactatctgaagagggtcaacctagatgaatggt gttccatttagtagttgaggaagaacccatgaggtttagaaagc agacaagcatgtggcaagttctggagtcagtggtaaaaattaaa gaacccaactattactgtcacctaatgatctaatggagactgtg gagatgggctgcatttttttaatcttctccagaatgccaaaatg taaacacatatctgtgtgtgtgtgtgtgtgtgtgtgtgtgtgtg agagagagagagagagagagagagactgaagtttgtacaattag acattttataaaatgttttctgaaggacagtggctcacaatctt aagtttctaacattgtacaatgttgggagactttgtatacttta ttttctctttagcatattaaggaatctgagatgtcctacagtaa agaaatttgcattacatagttaaaatcagggttattcaaacttt ttgattattgaaacctttcttcattagttactagggttgaatga aactagtgttccacagaaaactatgggaaatgttgctaggcagt aaggacatggtgatttcagcatgtgcaatatttacagcgattgc acccatggaccaccctggcagtagtgaaataaccaaaaatgctg tcataactagtatggctatgagaaacacattggg RLBP1 INTRONIC 14 SEQUENCE AS ATTCTCCAGGTTGAGCCAGACCAATTTGATGGTAGATTTAGCAA STUFFER ATAAAAATACAGGACACCCAGTTAAATGTGAATTTCCGATGAAC SEQUENCE AGCAAATACTTTTTTAGTATTAAAAAAGTTCACATTTAGGCTCA (NT_010274.17) CGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAGATCA CCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAA CCCCATCTCCACTAAAAATACCAAAAATTAGCCAGGCGTGCTGG TGGGCACCTGTAGTTCCAGCTACTCAGGAGGCTAAGGCAGGAGA ATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGATCG CACCATTGCACTCTAGCCTGGGCGACAAGAACAAAACTCCATCT CAAAAAAAAAAAAAAAAAAAAAGTTCACATTTAACTGGGCATTC TGTATTTAATTGGTAATCTGAGATGGCAGGGAACAGCATCAGCA TGGTGTGAGGGATAGGCATTTTTTCATTGTGTACAGCTTGTAAA TCAGTATTTTTAAAACTCAAAGTTAATGGCTTGGGCATATTTAG AAAAGAGTTGCCGCACGGACTTGAACCCTGTATTCCTAAAATCT AGGATCTTGTTCTGATGGTCTGCACAACTGGCTGGGGGTGTCCA GCCACTGTCCCTCTTGCCTGGGCTCCCCAGGGCAGTTCTGTCAG CCTCTCCATTTCCATTCCTGTTCCAGCAAAACCCAACTGATAGC ACAGCAGCATTTCAGCCTGTCTACCTCTGTGCCCACATACCTGG ATGTCTACCAGCCAGAAAGGTGGCTTAGATTTGGTTCCTGTGGG TGGATTATGGCCCCCAGAACTTCCCTGTGCTTGCTGGGGGTGTG GAGTGGAAAGAGCAGGAAATGGGGGACCCTCCGATACTCTATGG GGGTCCTCCAAGTCTCTTTGTGCAAGTTAGGGTAATAATCAATA TGGAGCTAAGAAAGAGAAGGGGAACTATGCTTTAGAACAGGACA CTGTGCCAGGAGCATTGCAGAAATTATATGGTTTTCACGACAGT TCTTTTTGGTAGGTACTGTTATTATCCTCAGTTTGCAGATGAGG AAACTGAGACCCAGAAAGGTTAAATAACTTGCTAGGGTCACACA AGTCATAACTGACAAAGCCTGATTCAAACCCAGGTCTCCCTAAC CTTTAAGGTTTCTATGACGCCAGCTCTCCTAGGGAGTTTGTCTT CAGATGTCTTGGCTCTAGGTGTCAAAAAAAGACTTGGTGTCAGG CAGGCATAGGTTCAAGTCCCAACTCTGTCACTTACCAACTGTGA CTAGGTGATTGAACTGACCATGGAACCTGGTCACATGCAGGAGC AGGATGGTGAAGGGTTCTTGAAGGCACTTAGGCAGGACATTTAG GCAGGAGAGAAAACCTGGAAACAGAAGAGCTGTCTCCAAAAATA CCCACTGGGGAAGCAGGTTGTCATGTGGGCCATGAATGGGACCT GTTCTGG AMP BACTERIAL 15 BACKBONE ctgcctgcaggggcgcctgatgcggtattttctccttacgcatc tgtgcggtatttcacaccgcatacgtcaaagcaaccatagtacg cgccctgtagcggcgcattaagcgcggcgggtgtggtggttacg cgcagcgtgaccgctacacttgccagcgccttagcgcccgctcc tttcgctttcttcccttcctttctcgccacgttcgccggctttc cccgtcaagctctaaatcgggggctccctttagggttccgattt agtgctttacggcacctcgaccccaaaaaacttgatttgggtga tggttcacgtagtgggccatcgccctgatagacggtttttcgcc ctttgacgttggagtccacgttctttaatagtggactcttgttc caaactggaacaacactcaactctatctcgggctattcttttga tttataagggattttgccgatttcggtctattggttaaaaaatg agctgatttaacaaaaatttaacgcgaattttaacaaaatatta acgtttacaattttatggtgcactctcagtacaatctgctctga tgccgcatagttaagccagccccgacacccgccaacacccgctg acgcgccctgacgggcttgtctgctcccggcatccgcttacaga caagctgtgaccgtctccgggagctgcatgtgtcagaggttttc accgtcatcaccgaaacgcgcgagacgaaagggcctcgtgatac gcctatttttataggttaatgtcatgataataatggtttcttag acgtcaggtggcacttttcggggaaatgtgcgcggaacccctat ttgtttatttttctaaatacattcaaatatgtatccgctcatga gacaataaccctgataaatgcttcaataatattgaaaaaggaag agtatgagtattcaacatttccgtgtcgcccttattcccttttt tgcggcattttgccttcctgtttttgctcacccagaaacgctgg tgaaagtaaaagatgctgaagatcagttgggtgcacgagtgggt tacatcgaactggatctcaacagcggtaagatccttgagagttt tcgccccgaagaacgttttccaatgatgagcacttttaaagttc tgctatgtggcgcggtattatcccgtattgacgccgggcaagag caactcggtcgccgcatacactattctcagaatgacttggttga gtactcaccagtcacagaaaagcatcttacggatggcatgacag taagagaattatgcagtgctgccataaccatgagtgataacact gcggccaacttacttctgacaacgatcggaggaccgaaggagct aaccgcttttttgcacaacatgggggatcatgtaactcgccttg atcgttgggaaccggagctgaatgaagccataccaaacgacgag cgtgacaccacgatgcctgtagcaatggcaacaacgttgcgcaa actattaactggcgaactacttactctagcttcccggcaacaat taatagactggatggaggcggataaagttgcaggaccacttctg cgctcggcccttccggctggctggtttattgctgataaatctgg agccggtgagcgtgggtctcgcggtatcattgcagcactggggc cagatggtaagccctcccgtatcgtagttatctacacgacgggg agtcaggcaactatggatgaacgaaatagacagatcgctgagat aggtgcctcactgattaagcattggtaactgtcagaccaagttt actcatatatactttagattgatttaaaacttcatttttaattt aaaaggatctaggtgaagatcctttttgataatctcatgaccaa aatcccttaacgtgagttttcgttccactgagcgtcagaccccg tagaaaagatcaaaggatcttcttgaaatcctttttttctgcgc gtaatctgctgcttgcaaacaaaaaaaccaccgctaccagcggt ggtttgtttgccggatcaagagctaccaactctttttccgaagg taactggcttcagcagagcgcagataccaaatactgttcttcta gtgtagccgtagttaggccaccacttcaagaactctgtagcacc gcctacatacctcgctctgctaatcctgttaccagtggctgctg ccagtggcgataagtcgtgtcttaccgggttggactcaagacga tagttaccggataaggcgcagcggtcgggctgaacggggggttc gtgcacacagcccagcttggagcgaacgacctacaccgaactga gatacctacagcgtgagctatgagaaagcgccacgcttcccgaa gggagaaaggcggacaggtatccggtaagcggcagggtcggaac aggagagcgcacgagggagcttccagggggaaacgcctggtatc tttatagtcctgtcgggtttcgccacctctgacttgagcgtcga tttttgtgatgctcgtcaggggggcggagcctatggaaaaacgc cagcaacgcggcctttttacggttcctggccttttgctggcctt ttgctcacatgtcctgcaggcag 5′ ITR - 16 STRATAGENE Ctgcgcgctcgctcgctcactgaggccgcccgggcaaagcccgg gcgtcgggcgacctttggtcgcccggcctcagtgagcgagcgag cgcgcagagagggagtggccaactccatcactaggggttcct 5′ ITR - NCBI 17 (AF043303) Ttggccactccctctctgcgcgctcgctcgctcactgaggccgg gcgaccaaaggtcgcccgacgcccgggctttgcccgggcggcct cagtgagcgagcgagcgcgcagagagggagtggccaactccatc actaggggttcct AAV2 CAPSID 18 CODING SEQUENCE atggctgccgatggttatcttccagattggctcgaggacactct ctctgaaggaataagacagtggtggaagctcaaacctggcccac caccaccaaagcccgcagagcggcataaggacgacagcaggggt cttgtgcttcctgggtacaagtacctcggacccttcaacggact cgacaagggagagccggtcaacgaggcagacgccgcggccctcg agcacgacaaagcctacgaccggcagctcgacagcggagacaac ccgtacctcaagtacaaccacgccgacgcggagtttcaggagcg ccttaaagaagatacgtcttttgggggcaacctcggacgagcag tcttccaggcgaaaaagagggttcttgaacctctgggcctggtt gaggaacctgttaagacggctccgggaaaaaagaggccggtaga gcactctcctgtggagccagactcctcctcgggaaccggaaagg cgggccagcagcctgcaagaaaaagattgaattttggtcagact ggagacgcagactcagtacctgacccccagcctctcggacagcc accagcagccccctctggtctgggaactaatacgatggctacag gcagtggcgcaccaatggcagacaataacgagggcgccgacgga gtgggtaattcctcgggaaattggcattgcgattccacatggat gggcgacagagtcatcaccaccagcacccgaacctgggccctgc ccacctacaacaaccacctctacaaacaaatttccagccaatca ggagcctcgaacgacaatcactactttggctacagcaccccttg ggggtattttgacttcaacagattccactgccacttttcaccac gtgactggcaaagactcatcaacaacaactggggattccgaccc aagagactcaacttcaagctctttaacattcaagtcaaagaggt cacgcagaatgacggtacgacgacgattgccaataaccttacca gcacggttcaggtgtttactgactcggagtaccagctcccgtac gtcctcggctcggcgcatcaaggatgcctcccgccgttcccagc agacgtcttcatggtgccacagtatggatacctcaccctgaaca acgggagtcaggcagtaggacgctcttcattttactgcctggag tactttccttctcagatgctgcgtaccggaaacaactttacctt cagctacacttttgaggacgttcctttccacagcagctacgctc acagccagagtctggaccgtctcatgaatcctctcatcgaccag tacctgtattacttgagcagaacaaacactccaagtggaaccac cacgcagtcaaggcttcagttttctcaggccggagcgagtgaca ttcgggaccagtctaggaactggcttcctggaccctgttaccgc cagcagcgagtatcaaagacatctgcggataacaacaacagtga atactcgtggactggagctaccaagtaccacctcaatggcagag actctctggtgaatccgggcccggccatggcaagccacaaggac gatgaagaaaagttttttcctcagagcggggttctcatctttgg gaagcaaggctcagagaaaacaaatgtggacattgaaaaggtca tgattacagacgaagaggaaatcaggacaaccaatcccgtggct acggagcagtatggttctgtatctaccaacctccagagaggcaa cagacaagcagctaccgcagatgtcaacacacaaggcgttcttc caggcatggtctggcaggacagagatgtgtaccttcaggggccc atctgggcaaagattccacacacggacggacattttcacccctc tcccctcatgggtggattcggacttaaacaccctcctccacaga ttctcatcaagaacaccccggtacctgcgaatccttcgaccacc ttcagtgcggcaaagtttgcttccttcatcacacagtactccac gggacaggtcagcgtggagatcgagtgggagctgcagaaggaaa acagcaaacgctggaatcccgaaattcagtacacttccaactac aacaagtctgttaatgtggactttactgtggacactaatggcgt gtattcagagcctcgccccattggcaccagatacctgactcgta atctgtaa AAV2 CAPSID 19 SEQUENCE (VP1) maadgylpdwledtlsegirqwwklkpgppppkpaerhkddsrg lvlpgykylgpfngldkgepvneadaaalehdkaydrqldsgdn pylkynhadaefqerlkedtsfggnlgravfqakkrvleplglv eepvktapgkkrpvehspvepdsssgtgkagqqparkrlnfgqt gdadsvpdpqplgqppaapsglgtntmatgsgapmadnnegadg vgnssgnwhcdstwmgdrvittstrtwalptynnhlykqissqs gasndnhyfgystpwgyfdfnrfhchfsprdwqrlinnnwgfrp krlnfklfniqvkevtqndgtttiannltstvqvftdseyqlpy vlgsahqgclppfpadvfmvpqygyltlnngsqavgrssfycle yfpsqmlrtgnnftfsytfedvpfhssyahsqsldrlmnplidq ylyylsrtntpsgtttqsrlqfsqagasdirdqsrnwlpgpcyr qqrvsktsadnnnseyswtgatkyhlngrdslvnpgpamashkd deekffpqsgvlifgkqgsektnvdiekvmitdeeeirttnpva teqygsvstnlqrgnrqaatadvntqgvlpgmvwqdrdvylqgp iwakiphtdghfhpsplmggfglkhpppqilikntpvpanpstt fsaakfasfitqystgqvsveiewelqkenskrwnpeiqytsny nksvnvdftvdtngvyseprpigtryltrnl AAV2 CAPSID 68 SEQUENCE (VP2) mapgkkrpvehspvepdsssgtgkagqqparkrlnfgqtgdads vpdpqplgqppaapsglgtntmatgsgapmadnnegadgvgnss gnwhcdstwmgdrvittstrtwalptynnhlykqissqsgasnd nhyfgystpwgyfdfnrfhchfsprdwqrlinnnwgfrpkrlnf klfniqvkevtqndgtttiannltstvqvftdseyqlpyvlgsa hqgclppfpadvfmvpqygyltlnngsqavgrssfycleyfpsq mlrtgnnftfsytfedvpfhssyahsqsldrlmnplidqylyyl srtntpsgtttqsrlqfsqagasdirdqsrnwlpgpcyrqqrvs ktsadnnnseyswtgatkyhlngrdslvnpgpamashkddeekf fpqsgvlifgkqgsektnvdiekvmitdeeeirttnpvateqyg svstnlqrgnrqaatadvntqgvlpgmvwqdrdvylqgpiwaki phtdghfhpsplmggfglkhpppqilikntpvpanpsttfsaak fasfitqystgqvsveiewelqkenskrwnpeiqytsnynksvn vdftvdtngvyseprpigtryltrnl AAV2 CAPSID 69 SEQUENCE (VP3) matgsgapmadnnegadgvgnssgnwhcdstwmgdrvittstrt walptynnhlykqissqsgasndnhyfgystpwgyfdfnrfhch fsprdwqrlinnnwgfrpkrlnfklfniqvkevtqndgtttian nltstvqvftdseyqlpyvlgsahqgclppfpadvfmvpqygyl tlnngsqavgrssfycleyfpsqmlrtgnnftfsytfedvpfhs syahsqsldrlmnplidqylyylsrtntpsgtttqsrlqfsqag asdirdqsrnwlpgpcyrqqrvsktsadnnnseyswtgatkyhl ngrdslvnpgpamashkddeekffpqsgvlifgkqgsektnvdi ekvmitdeeeirttnpvateqygsvstnlqrgnrqaatadvntq gvlpgmvwqdrdvylqgpiwakiphtdghfhpsplmggfglkhp ppqilikntpvpanpsttfsaakfasfitqystgqvsveiewel qkenskrwnpeiqytsnynksvnvdftvdtngvyseprpigtry ltrnl AAV8 CAPSID 20 CODING SEQUENCE atggctgccgatggttatcttccagattggctcgaggacaacct ctctgagggcattcgcgagtggtgggcgctgaaacctggagccc cgaagcccaaagccaaccagcaaaagcaggacgacggccggggt ctggtgcttcctggctacaagtacctcggacccttcaacggact cgacaagggggagcccgtcaacgcggcggacgcagcggccctcg agcacgacaaggcctacgaccagcagctgcaggcgggtgacaat ccgtacctgcggtataaccacgccgacgccgagtttcaggagcg tctgcaagaagatacgtcttttgggggcaacctcgggcgagcag tcttccaggccaagaagcgggttctcgaacctctcggtctggtt gaggaaggcgctaagacggctcctggaaagaagagaccggtaga gccatcaccccagcgttctccagactcctctacgggcatcggca agaaaggccaacagcccgccagaaaaagactcaattttggtcag actggcgactcagagtcagttccagaccctcaacctctcggaga acctccagcagcgccctctggtgtgggacctaatacaatggctg caggcggtggcgcaccaatggcagacaataacgaaggcgccgac ggagtgggtagttcctcgggaaattggcattgcgattccacatg gctgggcgacagagtcatcaccaccagcacccgaacctgggccc tgcccacctacaacaaccacctctacaagcaaatctccaacggg acatcgggaggagccaccaacgacaacacctacttcggctacag caccccctgggggtattttgactttaacagattccactgccact tttcaccacgtgactggcagcgactcatcaacaacaactgggga ttccggcccaagagactcagcttcaagctcttcaacatccaggt caaggaggtcacgcagaatgaaggcaccaagaccatcgccaata acctcaccagcaccatccaggtgtttacggactcggagtaccag ctgccgtacgttctcggctctgcccaccagggctgcctgcctcc gttcccggcggacgtgttcatgattccccagtacggctacctaa cactcaacaacggtagtcaggccgtgggacgctcctccttctac tgcctggaatactttccttcgcagatgctgagaaccggcaacaa cttccagtttacttacaccttcgaggacgtgcctttccacagca gctacgcccacagccagagcttggaccggctgatgaatcctctg attgaccagtacctgtactacttgtctcggactcaaacaacagg aggcacggcaaatacgcagactctgggcttcagccaaggtgggc ctaatacaatggccaatcaggcaaagaactggctgccaggaccc tgttaccgccaacaacgcgtctcaacgacaaccgggcaaaacaa caatagcaactttgcctggactgctgggaccaaataccatctga atggaagaaattcattggctaatcctggcatcgctatggcaaca cacaaagacgacgaggagcgtttttttcccagtaacgggatcct gatttttggcaaacaaaatgctgccagagacaatgcggattaca gcgatgtcatgctcaccagcgaggaagaaatcaaaaccactaac cctgtggctacagaggaatacggtatcgtggcagataacttgca gcagcaaaacacggctcctcaaattggaactgtcaacagccagg gggccttacccggtatggtctggcagaaccgggacgtgtacctg cagggtcccatctgggccaagattcctcacacggacggcaactt ccacccgtctccgctgatgggcggctttggcctgaaacatcctc cgcctcagatcctgatcaagaacacgcctgtacctgcggatcct ccgaccaccttcaaccagtcaaagctgaactctttcatcacgca atacagcaccggacaggtcagcgtggaaattgaatgggagctgc agaaggaaaacagcaagcgctggaaccccgagatccagtacacc tccaactactacaaatctacaagtgtggactttgctgttaatac agaaggcgtgtactctgaaccccgccccattggcacccgttacc tcacccgtaatctgtaa AAV8 CAPSID 21 SEQUENCE (VP1) maadgylpdwlednlsegirewwalkpgapkpkanqqkqddgrg lvlpgykylgpfngldkgepvnaadaaalehdkaydqqlqagdn pylrynhadaefqerlqedtsfggnlgravfqakkrvleplglv eegaktapgkkrpvepspqrspdsstgigkkgqqparkrlnfgq tgdsesvpdpqplgeppaapsgvgpntmaagggapmadnnegad gvgsssgnwhcdstwlgdrvittstrtwalptynnhlykqisng tsggatndntyfgystpwgyfdfnrfhchfsprdwqrlinnnwg frpkrlsfklfniqvkevtqnegtktiannltstiqvftdseyq lpyvlgsahqgclppfpadvfmipqygyltlnngsqavgrssfy cleyfpsqmlrtgnnfqftytfedvpfhssyahsqsldrlmnpl idqylyylsrtqttggtantqtlgfsqggpntmanqaknwlpgp cyrqqrvstttgqnnnsnfawtagtkyhlngrnslanpgiamat hkddeerffpsngilifgkqnaardnadysdvmltseeeikttn pvateeygivadnlqqqntapqigtvnsqgalpgmvwqnrdvyl qgpiwakiphtdgnfhpsplmggfglkhpppqilikntpvpadp pttfnqsklnsfitqystgqvsveiewelqkenskrwnpeiqyt snyykstsvdfavntegvyseprpigtryltrnl AAV8 CAPSID 70 SEQUENCE (VP2) mapgkkrpvepspqrspdsstgigkkgqqparkrlnfgqtgdse svpdpqplgeppaapsgvgpntmaagggapmadnnegadgvgss sgnwhcdstwlgdrvittstrtwalptynnhlykqisngtsgga tndntyfgystpwgyfdfnrfhchfsprdwqrlinnnwgfrpkr lsfklfniqvkevtqnegtktiannltstiqvftdseyqlpyvl gsahqgclppfpadvfmipqygyltlnngsqavgrssfycleyf psqmlrtgnnfqftytfedvpfhssyahsqsldrlmnplidqyl yylsrtqttggtantqtlgfsqggpntmanqaknwlpgpcyrqq rvstttgqnnnsnfawtagtkyhlngrnslanpgiamathkdde erffpsngilifgkqnaardnadysdvmltseeeikttnpvate eygivadnlqqqntapqigtvnsqgalpgmvwqnrdvylqgpiw akiphtdgnfhpsplmggfglkhpppqilikntpvpadppttfn qsklnsfitqystgqvsveiewelqkenskrwnpeiqytsnyyk stsvdfavntegvyseprpigtryltrnl AAV8 CAPSID 71 SEQUENCE (VP3) maagggapmadnnegadgvgsssgnwhcdstwlgdrvittstrt walptynnhlykqisngtsggatndntyfgystpwgyfdfnrfh chfsprdwqrlinnnwgfrpkrlsfklfniqvkevtqnegtkt annltstiqvftdseyqlpyvlgsahqgclppfpadvfmipqyg yltlnngsqavgrssfycleyfpsqmlrtgnnfqftytfedvpf hssyahsqsldrlmnplidqylyylsrtqttggtantqtlgfsq ggpntmanqaknwlpgpcyrqqrvstttgqnnnsnfawtagtky hlngrnslanpgiamathkddeerffpsngilifgkqnaardna dysdvmltseeeikttnpvateeygivadnlqqqntapqigtvn sqgalpgmvwqnrdvylqgpiwakiphtdgnfhpsplmggfglk hpppqilikntpvpadppttfnqsklnsfitqystgqvsveiew elqkenskrwnpeiqytsnyykstsvdfavntegvyseprpigt ryltrnl CVM ENHANCER 22 AND CBA ACTAGTTATTAATAGTAATCAATTACGGGGTCATTAGTTCATAG PROMOTER CCCATATATGGAGTTCCGCGTTACATAACTTACGGTAAATGGCC (GENBANK CGCCTGGCTGACCGCCCAACGACCCCCGCCCATTGACGTCAATA ACCESSION ATGACGTATGTTCCCATAGTAACGCCAATAGGGACTTTCCATTG DD215332 FROM ACGTCAATGGGTGGAGTATTTACGGTAAACTGCCCACTTGGCAG BP 1-BP 1616) TACATCAAGTGTATCATATGCCAAGTACGCCCCCTATTGACGTC AATGACGGTAAATGGCCCGCCTGGCATTATGCCCAGTACATGAC CTTATGGGACTTTCCTACTTGGCAGTACATCTACGTATTAGTCA TCGCTATTACCATGGTCGAGGTGAGCCCCACGTTCTGCTTCACT CTCCCCATCTCCCCCCCCTCCCCACCCCCAATTTTGTATTTATT TATTTTTTAATTATTTTGTGCAGCGATGGGGGCGGGGGGGGGGG GGGGGCGCGCGCCAGGCGGGGCGGGGCGGGGCGAGGGGCGGGGC GGGGCGAGGCGGAGAGGTGCGGCGGCAGCCAATCAGAGCGGCGC GCTCCGAAAGTTTCCTTTTATGGCGAGGCGGCGGCGGCGGCGGC CCTATAAAAAGCGAAGCGCGCGGCGGGCGGGGAGTCGCTGCGAC GCTGCCTTCGCCCCGTGCCCCGCTCCGCCGCCGCCTCGCGCCGC CCGCCCCGGCTCTGACTGACCGCGTTACTCCCACAGGTGAGCGG GCGGGACGGCCCTTCTCCTCCGGGCTGTAATTAGCGCTTGGTTT AATGACGGCTTGTTTCTTTTCTGTGGCTGCGTGAAAGCCTTGAG GGGCTCCGGGAGGGCCCTTTGTGCGGGGGGAGCGGCTCGGGGGG TGCGTGCGTGTGTGTGTGCGTGGGGAGCGCCGCGTGCGGCTCCG CGCTGCCCGGCGGCTGTGAGCGCTGCGGGCGCGGCGCGGGGCTT TGTGCGCTCCGCAGTGTGCGCGAGGGGAGCGCGGCCGGGGGCGG TGCCCCGCGGTGCGGGGGGGGCTGCGAGGGGAACAAAGGCTGCG TGCGGGGTGTGTGCGTGGGGGGGTGAGCAGGGGGTGTGGGCGCG TCGGTCGGGCTGCAACCCCCCCTGCACCCCCCTCCCCGAGTTGC TGAGCACGGCCCGGCTTCGGGTGCGGGGCTCCGTACGGGGCGTG GCGCGGGGCTCGCCGTGCCGGGCGGGGGGTGGCGGCAGGTGGGG GTGCCGGGCGGGGCGGGGCCGCCTCGGGCCGGGGAGGGCTCGGG GGAGGGGCGCGGCGGCCCCCGGAGCGCCGGCGGCTGTCGAGGCG CGGCGAGCCGCAGCCATTGCCTTTTATGGTAATCGTGCGAGAGG GCGCAGGGACTTCCTTTGTCCCAAATCTGTGCGGAGCCGAAATC TGGGAGGCGCCGCCGCACCCCCTCTAGCGGGCGCGGGGCGAAGC GGTGCGGCGCCGGCAGGAAGGAAATGGGCGGGGAGGGCCTTCGT GCGTCGCCGCGCCGCCGTCCCCTTCTCCCTCTCCAGCCTCGGGG CTGTCCGCGGGGGGACGGCTGCCTTCGGGGGGGACGGGGCAGGG CGGGGTTCGGCTTCTGGCGTGTGACCGGCGGC REVERSE 23 COMPLEMENT OF CCAGAACAGGTCCCATTCATGGCCCACATGACAACCTGCTTCCC RLBP1 INTRONIC CAGTGGGTATTTTTGGAGACAGCTCTTCTGTTTCCAGGTTTTCT SEQUENCE AS CTCCTGCCTAAATGTCCTGCCTAAGTGCCTTCAAGAACCCTTCA STUFFER CCATCCTGCTCCTGCATGTGACCAGGTTCCATGGTCAGTTCAAT SEQUENCE CACCTAGTCACAGTTGGTAAGTGACAGAGTTGGGACTTGAACCT (NT_010274.17) ATGCCTGCCTGACACCAAGTCTTTTTTTGACACCTAGAGCCAAG ACATCTGAAGACAAACTCCCTAGGAGAGCTGGCGTCATAGAAAC CTTAAAGGTTAGGGAGACCTGGGTTTGAATCAGGCTTTGTCAGT TATGACTTGTGTGACCCTAGCAAGTTATTTAACCTTTCTGGGTC TCAGTTTCCTCATCTGCAAACTGAGGATAATAACAGTACCTACC AAAAAGAACTGTCGTGAAAACCATATAATTTCTGCAATGCTCCT GGCACAGTGTCCTGTTCTAAAGCATAGTTCCCCTTCTCTTTCTT AGCTCCATATTGATTATTACCCTAACTTGCACAAAGAGACTTGG AGGACCCCCATAGAGTATCGGAGGGTCCCCCATTTCCTGCTCTT TCCACTCCACACCCCCAGCAAGCACAGGGAAGTTCTGGGGGCCA TAATCCACCCACAGGAACCAAATCTAAGCCACCTTTCTGGCTGG TAGACATCCAGGTATGTGGGCACAGAGGTAGACAGGCTGAAATG CTGCTGTGCTATCAGTTGGGTTTTGCTGGAACAGGAATGGAAAT GGAGAGGCTGACAGAACTGCCCTGGGGAGCCCAGGCAAGAGGGA CAGTGGCTGGACACCCCCAGCCAGTTGTGCAGACCATCAGAACA AGATCCTAGATTTTAGGAATACAGGGTTCAAGTCCGTGCGGCAA CTCTTTTCTAAATATGCCCAAGCCATTAACTTTGAGTTTTAAAA ATACTGATTTACAAGCTGTACACAATGAAAAAATGCCTATCCCT CACACCATGCTGATGCTGTTCCCTGCCATCTCAGATTACCAATT AAATACAGAATGCCCAGTTAAATGTGAACTTTTTTTTTTTTTTT TTTTTTGAGATGGAGTTTTGTTCTTGTCGCCCAGGCTAGAGTGC AATGGTGCGATCTCAGCTCACTGCAACCTCTGCCTCCCAGGTTC AAGCAATTCTCCTGCCTTAGCCTCCTGAGTAGCTGGAACTACAG GTGCCCACCAGCACGCCTGGCTAATTTTTGGTATTTTTAGTGGA GATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGA CCTCAGGTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATT ACAGGCGTGAGCCTAAATGTGAACTTTTTTAATACTAAAAAAGT ATTTGCTGTTCATCGGAAATTCACATTTAACTGGGTGTCCTGTA TTTTTATTTGCTAAATCTACCATCAAATTGGTCTGGCTCAACCT GGAGAAT EGFP SEQUENCE 24 ATGGTGAGCAAGGGCGAGGAGCTGTTCACCGGGGTGGTGCCCAT CCTGGTCGAGCTGGACGGCGACGTAAACGGCCACAAGTTCAGCG TGTCCGGCGAGGGCGAGGGCGATGCCACCTACGGCAAGCTGACC CTGAAGTTCATCTGCACCACCGGCAAGCTGCCCGTGCCCTGGCC CACCCTCGTGACCACCCTGACCTACGGCGTGCAGTGCTTCAGCC GCTACCCCGACCACATGAAGCAGCACGACTTCTTCAAGTCCGCC ATGCCCGAAGGCTACGTCCAGGAGCGCACCATCTTCTTCAAGGA CGACGGCAACTACAAGACCCGCGCCGAGGTGAAGTTCGAGGGCG ACACCCTGGTGAACCGCATCGAGCTGAAGGGCATCGACTTCAAG GAGGACGGCAACATCCTGGGGCACAAGCTGGAGTACAACTACAA CAGCCACAACGTCTATATCATGGCCGACAAGCAGAAGAACGGCA TCAAGGTGAACTTCAAGATCCGCCACAACATCGAGGACGGCAGC GTGCAGCTCGCCGACCACTACCAGCAGAACACCCCCATCGGCGA CGGCCCCGTGCTGCTGCCCGACAACCACTACCTGAGCACCCAGT CCGCCCTGAGCAAAGACCCCAACGAGAAGCGCGATCACATGGTC CTGCTGGAGTTCGTGACCGCCGCCGGGATCACTCTCGGCATGGA CGAGCTGTACAAGTAA GFP AMINO ACID 25 SEQUENCE MVSKGEELFTGVVPILVELDGDVNGHKFSVSGEGEGDATYGKLT LKFICT TGKLPVPWPTLVTTLTYGVQCFSRYPDHMKQHDFFKSAMPEGYV QERTIF FKDDGNYKTRAEVKFEGDTLVNRIELKGIDFKEDGNILGHKLEY NYNSHN VYIMADKQKNGIKVNFKIRHNIEDGSVQLADHYQQNTPIGDGPV LLPDNH YLSTQSALSKDPNEKRDHMVLLEFVTAAGITLGMDELYK SC5′ITR 36 CTGCGCGCTCGCTCGCTCACTGAGGCCGCCCGGGCAAAGCCCGG GCGTCGGGCGACCTTTGGTCGCCCGGCCTCAGTGAGCGAGCGAG CGCGCAGAGAGGGAGTGGCCAACTCCATCACTAGGGGTTCCT MACACA MULATTA 37 (RHESUS MONKEY) ATGTCAGAAGGGGTGGGCACGTTCCGCATGGTACCTGAAGAGGA RLBP1 CDS ACAGGAGCTCCGTGCCCAACTGGAGCAGCTCACAACCAAGGACC XM_001091538 ATGGACCTGTCTTTGGCCCGTGCAGCCAGCTGCCCCGCCACACC TTGCAGAAGGCCAAAGATGAGCTGAATGAGAGAGAGGAGACCCG GGAGGAGGCAGTGCGAGAGCTGCAGGAGATGGTGCAGGCGCAGG CGGCCTCGGGGGAGGAGCTGGCCGTGGCCGTGGCGGAGAGGGTG CAAGAGAAGGACAGCGGCTTCTTCCTGCGCTTCATCCGCGCGCG AAAGTTCAACGTGGGCCGTGCCTATGAGCTGCTCAGAGGCTATG TGAATTTCCGGCTGCAGTACCCTGAGCTCTTTGACAGCCTGTCC CCAGAGGCTGTCCGCTGTACCATTGAAGCTGGCTACCCTGGTGT CCTCTCTAGTCGGGACAAGTATGGCCGAGTGGTCATGCTCTTCA ACATTGAGAACTGGCAAAGTCAAGAAATCACCTTCGATGAGATC TTGCAGGCATATTGCTTCATCCTGGAGAAGCTGCTGGAGAATGA GGAAACTCAAATTAATGGATTCTGCATCATTGAGAACTTCAAGG GCTTTACCATGCAGCAGGCTGCTAGTCTCCGCACTTCAGATCTC AGGAAGATGGTGGACATGCTCCAGGATTCCTTCCCAGCCCGGTT CAAAGCCATCCACTTCATCCACCAGCCATGGTACTTCACCACGA CCTACAATGTGGTCAAGCCCTTCTTGAAGAGCAAGCTGCTTGAG AGGGTCTTTGTCCACGGGGAGGACCTCTCTGGTTTCTACCAGGA GATTGATGAGAACATCCTGCCCTCTGACTTTGGGGGCACGCTGC CCAAGTATGATGGCAAAGCTGTTGCTGAGCAGCTCTTTGGCCCC CGGGCCCAAGCTGAGAACACAGCCTTCTGA MACACA MULATTA 38 (RHESUS MONKEY) MSEGVGTFRMVPEEEQELRAQLEQLTTKDHGPVFGPCSQLPRHT RLBP1 GENE LQKAKDELNEREETREEAVRELQEMVQAQAASGEELAVAVAERV PRODUCT QEKDSGFFLRFIRARKFNVGRAYELLRGYVNFRLQYPELFDSLS (CELLULAR PEAVRCTIEAGYPGVLSSRDKYGRVVMLFNIENWQSQEITFDEI RETINALDEHYDE LQAYCFILEKLLENEETQINGFCIIENFKGFTMQQAASLRTSDL BINDING PROTEIN - RKMVDMLQDSFPARFKAIHFIHQPWYFTTTYNVVKPFLKSKLLE CRALBP) RVFVHGEDLSGFYQEIDENILPSDFGGTLPKYDGKAVAEQLFGP RAQAENTAF BOS TAURUS 39 RLBP1 CDS ATGTCAGAGGGGGCGGGCACGTTCCGCATGGTCCCTGAAGAGGA NM_174451 ACAGGAGCTCCGTGCCCAACTGGAGAGGCTTACGACCAAAGACC ATGGACCTGTCTTTGGCCCGTGCAGCCAGCTGCCCCGCCACACC TTGCAGAAGGCCAAGGACGAGCTGAATGAAAAGGAAGAGACCCG GGAAGAGGCAGTGCGGGAGCTACAGGAGCTGGTGCAGGCGGAGG CCGCCTCGGGGCAGGAGCTGGCCGTGGCCGTGGCGGAGAGGGTG CAGGGAAAAGACAGTGCCTTCTTCCTGCGCTTCATCCGCGCGCG CAAGTTCCACGTGGGGCGCGCCTACGAGCTGCTCAGAGGCTACG TGAACTTCCGGCTGCAGTACCCAGAGCTCTTCGACAGCCTGTCC CCAGAGGCTGTCCGCTGCACCGTTGAGGCTGGCTACCCTGGTGT CCTCTCCACGCGGGACAAGTATGGCCGAGTGGTCATGCTCTTCA ATATTGAGAACTGGGACTCTGAAGAAATCACCTTTGATGAGATC TTGCAGGCATACTGCGTCATCCTGGAGAAGCTACTGGAGAATGA GGAGACTCAAATTAATGGCTTTTGCATCATTGAGAACTTCAAGG GCTTCACCATGCAGCAGGCTGCCGGACTTCGGCCTTCCGATC TCAGAAAGATGGTGGACATGCTCCAGGATTCCTTCCCAGCTCGG TTCAAAGCCATCCACTTCATCTACCAGCCCTGGTACTTCACCAC CACCTACAACGTGGTCAAGCCCTTCTTGAAGAGCAAATTGCTCC AGAGGGTATTTGTCCATGGAGAAGACCTCTCCAGCTTCTACCAG GAGTTTGACGAGGACATCCTGCCCTCCGACTTTGGGGGTACACT GCCCAAGTATGATGGCAAGGCCGTTGCTGAGCAGCTCTTTGGTC CTCGGGACCAAACTGAGAACACAGCCTTCTGA BOS TAURUS 40 RLBP1 GENE MSEGAGTFRMVPEEEQELRAQLERLTTKDHGPVFGPCSQLPRHT PRODUCT LQKAKDELNEKEETREEAVRELQELVQAEAASGQELAVAVAERV (CELLULAR QGKDSAFFLRFIRARKFHVGRAYELLRGYVNFRLQYPELFDSLS RETINALDEHYDE PEAVRCTVEAGYPGVLSTRDKYGRVVMLFNIENWDSEEITFDEI BINDING PROTEIN - LQAYCVILEKLLENEETQINGFCIIENFKGFTMQQAAGLRPSDL CRALBP) RKMVDMLQDSFPARFKAIHFIYQPWYFTTTYNVVKPFLKSKLLQ RVFVHGEDLSSFYQEFDEDILPSDFGGTLPKYDGKAVAEQLFGP RDQTENTAF CANIS LUPUS 41 FAMILIARIS ATGTCAGAAGGCGTGGGCACATTCCGTGTGGTCCCTGAAGAGGA RLBP1 CDS ACAGGAGCTCCGTGCCCAGCTGGAGCGGCTTACAACCAAGGACC XM_549634 ATGGGCCTGTCTTTGGCCCTTGCAGCCAGCTCCCTCGTCATACC TTACAGAAGGCCAAGGACGAGCTGAACGAGAGGGAGGAGACCCG GGAGGAGGTGGTGCGAGAGCTGCAGGAGCTGGTGCAGGCACAGG CTGCCACCGGGCAGGAGCTGGCCAGGGCGGTGGCTGAGAGGGTG CAGGGAAGGGACAGTGCCTTCTTCCTGCGCTTCATCCGCGCGCG GAAGTTCCATGTGGGGCGTGCCTACGAGCTGCTTCGAGGCTACG TGAACTTCCGGCTGCAGTACCCAGAGCTCTTCGACAGCCTGTCC CTGGAGGCTGTCCGTTGCACCGTCGAGGCCGGCTATCCTGGGGT CCTCCCCAGTCGGGACAAGTATGGCCGAGTGGTCATGCTCTTCA ACATCGAGAACTGGGACTCCGAAGAAATCACCTTCGATGAGATC TTGCAGGCATATTGTTTCATCCTGGAGAAGCTACTAGAGAATGA GGAAACTCAAATTAATGGCTTCTGCATTATTGAGAACTTTAAGG GCTTTACCATGCAGCAGGCTGCTGGACTTCGGGCTTCCGATCTC AGGAAGATGGTGGACATGCTCCAGGATTCCTTCCCAGCGCGGTT CAAAGCCATCCACTTCATTCACCAACCATGGTACTTCACCACCA CCTACAACATGGTCAAGCCCCTCCTGAAGAACAAGCTGCTCCAA AGAGTCTTTGTCCATGGAGATGACCTCTCTGGCTTCTTCCAGGA GATTGATGAAGACATACTGCCCGCTGACTTTGGGGGCACACTGC CCAAGTATGATGGCAAGGTGGTTGCTGAGCAGCTCTTTGGCCCC CGGGCCCAAGCTGAGAACACAGCCTTCTGA CANIS LUPUS 42 FAMILIARIS MSEGVGTFRVVPEEEQELRAQLERLTTKDHGPVFGPCSQLPRHT RLBP1 GENE LQKAKDELNEREETREEVVRELQELVQAQAATGQELARAVAERV PRODUCT QGRDSAFFLRFIRARKFHVGRAYELLRGYVNFRLQYPELFDSLS (CELLULAR LEAVRCTVEAGYPGVLPSRDKYGRVVMLFNIENWDSEEITFDEI RETINALDEHYDE LQAYCFILEKLLENEETQINGFCIIENFKGFTMQQAAGLRASDL BINDING PROTEIN - RKMVDMLQDSFPARFKAIHFIHQPWYFTTTYNMVKPLLKNKLLQ CRALBP) RVFVHGDDLSGFFQEIDEDILPADFGGTLPKYDGKVVAEQLFGP RAQAENTAF RATTUS 43 NORVEGICUS ATGTCAGAGGGGGTGGGCACATTCCGAATGGTCCCTGAAGAGGA RLBP1 CDS GCAGGAGCTCCGGGCACAGCTAGAACAGCTCACAACCAAGGATC NM_001106274.1 ATGGTCCTGTCTTTGGCCCATGCAGCCAGCTGCCCCGCCACACT TTGCAGAAGGCTAAGGATGAGCTGAATGAAAGGGAGGAAACCCG GGATGAGGCGGTGAGGGAGCTACAGGAGCTGGTCCAGGCACAGG CAGCTTCTGGGGAAGAGTTGGCCGTGGCAGTGGCTGAGAGGGTG CAGGCAAGAGACAGCGCCTTCCTCCTGCGCTTCATCCGTGCCCG AAAGTTTGATGTGGGCCGGGCTTATGAGCTGCTCAAAGGCTATG TGAACTTCCGGCTCCAGTACCCTGAACTCTTCGATAGCCTATC TATGGAGGCTCTCCGCTGCACTATCGAGGCCGGTTACCCTGGTG TCCTTTCCAGTCGGGACAAGTATGGTCGAGTGGTTATGCTCTTC AACATTGAAAACTGGCACTGTGAAGAAGTCACCTTTGATGAGAT CTTACAGGCATATTGTTTCATTCTGGAGAAACTGCTGGAGAACG AGGAAACCCAAATCAACGGCTTCTGTATTGTGGAGAACTTCAAG GGCTTCACCATGCAGCAGGCCGCGGGACTCCGCCCCTCCGATCT CAAGAAGATGGTGGACATGCTCCAGGATTCATTCCCAGCCAGGT TCAAAGCTATCCACTTCATCCACCAACCATGGTACTTCACCACC ACTTACAATGTGGTCAAGCCCTTCTTGAAGAACAAGTTGCTACA GAGGGTCTTCGTTCATGGAGATGACCTGGACGGCTTCTTCCAGG AGATTGATGAGAATATCTTGCCTGCTGACTTTGGGGGTACACTG CCCAAGTATGACGGCAAAGTTGTCGCTGAGCAGCTCTTCGGTCC CCGGGTTGAGGTTGAGAACACAGCCTTGTGA RATTUS 44 NORVEGICUS MSEGVGTFRMVPEEEQELRAQLEQLTTKDHGPVFGPCSQLPRHT RLBP1 GENE LQKAKDELNEREETRDEAVRELQELVQAQAASGEELAVAVAERV PRODUCT QARDSAFLLRFIRARKFDVGRAYELLKGYVNFRLQYPELFDSLS (CELLULAR MEALRCTIEAGYPGVLSSRDKYGRVVMLFNIENWHCEEVTFDEI RETINALDEHYDE LQAYCFILEKLLENEETQINGFCIVENFKGFTMQQAAGLRPS BINDING PROTEIN - DLKKMVDMLQDSFPARFKAIHFIHQPWYFTTTYNVVKPFLKNKL CRALBP) LQRVFVHGDDLDGFFQEIDENILPADFGGTLPKYDGKVVAEQLF GPRVEVENTAL MUS MUSCULUS 45 RLBP1 CDS ATGTCAGACGGGGTGGGCACTTTCCGCATGGTTCCTGAAGAGGA NM_020599.2 GCAGGAGCTCCGAGCACAACTGGAGCAGCTCACAACCAAGGATC ATGGTCCTGTCTTTGGCCCATGCAGCCAGCTGCCCCGCCACACT TTGCAGAAGGCCAAGGATGAGCTGAATGAAAAGGAGGAGACCCG GGAGGAAGCGGTGAGGGAGCTACAGGAGCTGGTACAGGCACAGG CAGCTTCTGGCGAGGAATTGGCCCTGGCAGTGGCTGAGAGGGTG CAGGCAAGAGACAGCGCCTTCCTCCTGCGCTTCATCCGTGCCCG CAAGTTCGATGTGGGTCGTGCTTATGAGCTGCTCAAAGGCTATG TGAACTTCCGCCTCCAGTACCCTGAACTCTTCGATAGTCTCTCC ATGGAGGCTCTCCGCTGCACTATCGAGGCCGGATACCCTGGTGT CCTTTCCAGTCGGGACAAGTATGGTCGAGTGGTTATGCTCTTCA ACATCGAAAACTGGCACTGTGAAGAAGTGACCTTTGATGAGATC TTACAGGCATATTGTTTCATTTTGGAGAAACTGCTGGAAAATGA GGAAACCCAAATCAACGGCTTCTGTATTGTTGAGAACTTCAAGG GCTTCACCATGCAGCAGGCAGCAGGGCTCCGCCCCTCGGATCTC AAGAAGATGGTGGACATGCTCCAGGATTCATTCCCAGCCAGGTT CAAAGCTATCCACTTCATCCACCAGCCATGGTACTTCACCACCA CCTATAATGTGGTCAAGCCCTTCTTGAAGAACAAGCTGCTACAG AGGGTCTTTGTTCACGGAGATGACCTGGATGGCTTCTTCCAGGA GATTGATGAGAACATCCTGCCTGCTGACTTTGGGGGTACACTGC CCAAGTACGACGGCAAAGTTGTTGCTGAGCAGCTCTTTGGTCCC CGGGCTGAAGTTGAGAACACAGCCTTATGA MUS MUSCULUS 46 RLBP1 GENE MSDGVGTFRMVPEEEQELRAQLEQLTTKDHGPVFGPCSQLPRHT PRODUCT LQKAKDELNEKEETREEAVRELQELVQAQAASGEELALAVAERV (CELLULAR QARDSAFLLRFIRARKFDVGRAYELLKGYVNFRLQYPELFDSLS RETINALDEHYDE MEALRCTIEAGYPGVLSSRDKYGRVVMLFNIENWHCEEVTFDEI BINDING PROTEIN - LQAYCFILEKLLENEETQINGFCIVENFKGFTMQQAAGLRPSDL CRALBP) KKMVDMLQDSFPARFKAIHFIHQPWYFTTTYNVVKPFLKNKLLQ RVFVHGDDLDGFFQEIDENILPADFGGTLPKYDGKVVAEQLFGP RAEVENTAL GALLUS GALLUS 47 RLBP1 CDS ATGTCTGCTGTTACGGGCACCTTCCGCATTGTCTCGGAAGAGGA NM_001024694.1 GCAGGCGCTGCGCACCAAACTGGAGCGCCTCACCACCAAGGACC ACGGCCCTGTTTTTGGGAGGTGCCAGCAGATCCCCCCTCACACC CTGCAGAAGGCAAAAGATGAGCTGAATGAGACGGAGGAGCAGAG GGAGGCAGCGGTCAAAGCGCTGCGGGAGCTGGTGCAGGAGCGGG CCGGCAGCGAGGATGTCTGCAAGGCAGTGGCAGAGAAGATGCAG GGGAAGGACGATTCCTTCTTCCTCCGCTTCATCCGTGCCCGCAA GTTTGACGTGCACAGGGCCTACGACCTGCTGAAAGGCTATGTGA ACTTTCGCCAGCAATACCCTGAACTCTTTGACAACCTGACCCCC GAGGCCGTGCGCAGCACCATCGAGGCGGGCTACCCCGGCATCCT GGCCAGCAGGGACAAATACGGGCGGGTAGTGATGCTCTTCAACA TCGAGAACTGGGACTACGAGGAGATCACCTTTGATGAGATCCTT CGTGCCTACTGCGTTATCTTGGAGAAGCTGCTGGAAAACGAAGA GACCCAGATCAATGGGTTCTGCATCATTGAGAACTTCAAGGGCT TCACCATGCAGCAGGCATCAGGGATCAAACCCTCCGAGCTCAAG AAGATGGTGGACATGCTACAGGACTCCTTCCCAGCGCGGTTCAA AGCTGTCCACTTCATCCACCAGCCCTGGTACTTCACCACTACCT ACAACGTGGTCAAACCGTTCCTGAAGAGCAAGCTGCTGGAGAGG GTGTTTGTGCACGGCGAGGAGCTGGAGTCCTTCTACCAGGAG ATCGATGCTGACATACTGCCAGCAGACTTCGGTGGCAACCTGCC CAAGTACGACGGCAAAGCAACTGCAGAGCAGCTCTTTGGGCCCC GCATTGAGGCTGAAGACACGGCACTTTAA GALLUS GALLUS 48 RLBP1 GENE MSAVTGTFRIVSEEEQALRTKLERLTTKDHGPVFGRCQQIPPHT PRODUCT LQKAKDELNETEEQREAAVKALRELVQERAGSEDVCKAVAEKMQ (CELLULAR GKDDSFFLRFIRARKFDVHRAYDLLKGYVNFRQQYPELFDNLTP RETINALDEHYDE EAVRSTIEAGYPGILASRDKYGRVVMLFNIENWDYEEITFDEIL BINDING PROTEIN - RAYCVILEKLLENEETQINGFCIIENFKGFTMQQASGIKPSELK CRALBP) KMVDMLQDSFPARFKAVHFIHQPWYFTTTYNVVKPFLKSKLLER NP_001019865.1 VFVHGEELESFYQEIDADILPADFGGNLPKYDGKATAEQLFGPR IEAEDTAL KAN-R BACTERIAL 49 BACKBONE CTGCCTGCAGGGTTCCATCCCAATGGCGCGTCAATTCACTGGCC GTCGTTTTACAACGTCGTGACTGGGAAAACCCTGGCGTTACCCA ACTTAATCGCCTTGCAGCACATCCCCCTTTCGCCAGCTGGCGTA ATAGCGAAGAGGCCCGCACCGATCGCCCTTCCCAACAGTTGCGC AGCCTGAATGGCGAATGGCGCCTGATGCGGTATTTTCTCCTTAC GCATCTGTGCGGTATTTCACACCGCATATGGTGCACTCTCAGTA CAATCTGCTCTGATGCCGCATAGTTAAGCCAGCCCCGACACCCG CCAACACCCGCTGACGCGCCCTGACGGGCTTGTCTGCTCCCGGC ATCCGCTTACAGACAAGCTGTGACCGTCTCCGGGAGCTGCATGT GTCAGAGGTTTTCACCGTCATCACCGAAACGCGCGAGACGAAAG GGCCTCGTGATACGCCTATTTTTATAGGTTAATGTCATGATAAT AATGGTTTCTTAGACGTCAGGTGGCACTTTTCGGGGAAATGTGC GCGGAACCCCTATTTGTTTATTTTTCTAAATACATTCAAATATG TATCCGCTCATGAGACAATAACCCTGATAAATGCTTCAATAATA TTGAAAAAGGAAGAGTATGAGCCATATTCAACGGGAAACGTCTT GCTCTAGGCCGCGATTAAATTCCAACATGGATGCTGATTTATAT GGGTATAAATGGGCTCGCGATAATGTCGGGCAATCAGGTGCGAC AATCTATCGATTGTATGGGAAGCCCGATGCGCCAGAGTTGTTTC TGAAACATGGCAAAGGTAGCGTTGCCAATGATGTTACAGATGAG ATGGTCAGACTAAACTGGCTGACGGAATTTATGCCTCTTCCGAC CATCAAGCATTTTATCCGTACTCCTGATGATGCATGGTTACTCA CCACTGCGATCCCTGGGAAAACAGCATTCCAGGTATTAGAAGAA TATCCTGATTCAGGTGAAAATATTGTTGATGCGCTGGCAGTGTT CCTGCGCCGGTTGCATTCGATTCCTGTTTGTAATTGTCCTTTTA ACAGCGATCGCGTATTTCGTCTCGCTCAGGCGCAATCACGAATG AATAACGGTTTGGTTGATGCGAGTGATTTTGATGACGAGCGTAA TGGCTGGCCTGTTGAACAAGTCTGGAAAGAAATGCATAAACTTT TGCCATTCTCACCGGATTCAGTCGTCACTCATGGTGATTTCTCA CTTGATAACCTTATTTTTGACGAGGGGAAATTAATAGGTTGTAT TGATGTTGGACGAGTCGGAATCGCAGACCGATACCAGGATCTTG CCATCCTATGGAACTGCCTCGGTGAGTTTTCTCCTTCATTACAG AAACGGCTTTTTCAAAAATATGGTATTGATAATCCTGATATGAA TAAATTGCAGTTTCATTTGATGCTCGATGAGTTTTTCTAACTGT CAGACCAAGTTTACTCATATATACTTTAGATTGATTTAAAACTT CATTTTTAATTTAAAAGGATCTAGGTGAAGATCCTTTTTGATAA TCTCATGACCAAAATCCCTTAACGTGAGTTTTCGTTCCACTGAG CGTCAGACCCCGTAGAAAAGATCAAAGGATCTTCTTGAGATCCT TTTTTTCTGCGCGTAATCTGCTGCTTGCAAACAAAAAAACCACC GCTACCAGCGGTGGTTTGTTTGCCGGATCAAGAGCTACCAACTC TTTTTCCGAAGGTAACTGGCTTCAGCAGAGCGCAGATACCAAAT ACTGTTCTTCTAGTGTAGCCGTAGTTAGGCCACCACTTCAAGAA CTCTGTAGCACCGCCTACATACCTCGCTCTGCTAATCCTGTTAC CAGTGGCTGCTGCCAGTGGCGATAAGTCGTGTCTTACCGGGTTG GACTCAAGACGATAGTTACCGGATAAGGCGCAGCGGTCGGGCTG AACGGGGGGTTCGTGCACACAGCCCAGCTTGGAGCGAACGACCT ACACCGAACTGAGATACCTACAGCGTGAGCTATGAGAAAGCGCC ACGCTTCCCGAAGGGAGAAAGGCGGACAGGTATCCGGTAAGCGG CAGGGTCGGAACAGGAGAGCGCACGAGGGAGCTTCCAGGGGGAA ACGCCTGGTATCTTTATAGTCCTGTCGGGTTTCGCCACCTCTGA CTTGAGCGTCGATTTTTGTGATGCTCGTCAGGGGGGCGGAGCCT ATGGAAAAACGCCAGCAACGCGGCCTTTTTACGGTTCCTGGCCT TTTGCTGGCCTTTTGCTCACATGTTCTTTCCTGCGTTATCCCCT GATTCTGTGGATAACCGTATTACCGCCTTTGAGTGAGCTGATAC CGCTCGCCGCAGCCGAACGACCGAGCGCAGCGAGTCAGTGAGCG AGGAAGCGGAAGAGCGCCCAATACGCAAACCGCCTCTCCCCGCG CGTTGGCCGATTCATTAATGCAGCTGGCACGACAGGTTTCCCGA CTGGAAAGCGGGCAGTGAGCGCAACGCAATTAATGTGAGTTAGC TCACTCATTAGGCACCCCAGGCTTTACACTTTATGCTTCCGGCT CGTATGTTGTGTGGAATTGTGAGCGGATAACAATTTCACACAGG AAACAGCTATGACCATGATTACGCCAAGCTCGGCGCGCCATTGG GATGGAACCCTGCAGGCAG Reverse 62 Complementary AGACATGATAAGATACATTGATGAGTTTGGACAAACCACAACTA sequence of GAATGCAGTGAAAAAAATGCTTTATTTGTGAAATTTGTGATGCT SV40polyA (SEQ ATTGCTTTATTTGTAACCATTATAAGCTGCAATAAACAAGTTAA ID NO: 8) CAACAACAATTGCATTCATTTTATGTTTCAGGTTCAGGGGGAGG TGTGGGAGGTTTTTTAAAGCAAGTAAAACCTCTACAAATGTGGT ATGGCTGATTATGATC Reverse 63 Complementary TCAGAAGGCTGTGTTCTCAGCTTGGGCCTGGGGGCCAAAGAGCT sequence of GCTCAGCAACGGCCTTGCCATCATACTTGGGCAGCGTGCCCCCG HUMAN RLBP1 AAGTCAGAGGGCAGGATGTTCTCATCGATCTCCTGGTAGAAACC GENE CDS (SEQ AGAAAGGTCATCCCCGTGGACAAAGACCCTCTCAAGCAGCTTGC ID NO: 7) TCTTCAAGAAGGGCTTGACCACATTGTAGGTCGTGGTGAAGTAC CATGGCTGGTGGATGAAGTGGATGGCTTTGAACCGGGCTGGGAA GGAATCCTGGAGCATGTCCACCATCTTCCTGAGATCTGAAGTCC GGAGACTAGCAGCCTGCTGCATGGTAAAGCCCTTGAAGTTCTCA ATGATGCAGAAGCCATTGATTTGAGTTTCCTCATTCTCCAGCAG CTTCTCCAGGATGAAGCAATATGCCTGCAAGATCTCATCAAAGG TGATTTCTTGACTTTGCCAGTTCTCAATGTTGAAGAGCATGACC ACTCGGCCATACTTGTCCCGACTAGAGAGGACACCAGGGTAGCC AGCTTCAATGGTGCAGCGGACAGCCTCTGGGGACAGGCTGTCAA AGAGCTCAGGGTACTGCAGCCGGAAATTCACATAGCCTCTGAGC AGCTCATAGGCACGGCCCACGTTGAACTTCCGTGCGCGGATGAA GCGCAGGAAGAAGCCGCTGTCCTTCTCTTGCACCCTCTCCGCCA CGGCCACCGCCAGCTCCTCCCCCGAGGCCGCCTGCGCCTGCACC ATCTCCTGCAGCTCTCGCACTGCCTCCTCCCGGGTCTCCTCTCT CTCGTTCAGCTCATCCTTGGCCTTCTGCAAGGTGTGGCGGGGCA GCTGGCTGCACGGGCCAAAGACAGGTCCATGGTCCTTGGTTGTG AGCTGCTCCAGTTGGGCACGGAGCTCCTGTTCCTCTTCAGGTAC CATGCGGAACGTGCCCACCCCTTCTGACAT Reverse 64 Complementary GGTGGC sequence of Added KOZAK (SEQ ID NO: 5) Reverse 65 Complementary GGATCCCGGGGCGGGTACAATTCCGCAGCTTTTAGAGCAGAAGT sequence of AACACTTCCGTACAGGCCTAGAAGTAAAGGCAACATCCACTGAG Modified GAGCAGTTCTTTGATTTGCACCACCACCGGATCCGGGACCTGAA SV40INTRON (SEQ ATAAAAGACAAAAAGACTAAACTTACCAGTTAACTTTCTGGTTT ID NO: 4) TTCAGTT Reverse 66 Complementary TCGGCAGCTCCTCCTTGGGGCTACCTGGTACCTGAATGTCCTGG sequence of AGCTCTAGAGGTTCCCTCCGCTGGAGGCGTGGTCCGGTCAGCAG Human RLBP1 GTTGGGATTAGTGTGTCATAAGGAACTTCTCACCGCCCACAGTT PROMOTER TCCGTTAAATCGGGCTCACAGGAGGCCCTCAGTGGGGCAAAGGA (short) (SEQ ID AGACCCAGAGAGAAAGGGGAGAGGGGAGAGGCCTGGGCCTGGCT NO: 3) GGAGGCGCATCAAAGCCCTCCTTTGTGTGCTCCTGCTCTGGAGT TCCTGCTCGGCCATGTGGAAGCCCGGCTGTGGGGCTGGGATCTG GGCCAGTCCCATTCCCTCTTTTCTCTGCCCTCTTTCTCCTCAAG ATCCCGGGGTGGGGTTGCTGAGAGAGCACCCCCCCCCCCCCACC ACCACCACCAGGGTAATAAGAGGTGAAGGGAAATCGTAAATATG ACTACATCTACAGTGGCAGCTCTGGCAAATCCAGGCCTATTGCC CACCCCTCCCCCAGCCAGCAGGACCTGGCATGGTAGTTTTCACC TCTGCAGTGAGTGGGGTCAGTTGAGAAATGTGGCTGGTTAAGGC CAAGCAGGGAGAGGACAA Reverse 67 Complementary TTACTTGTACAGCTCGTCCATGCCGAGAGTGATCCCGGCGGCGG sequence of TCACGAACTCCAGCAGGACCATGTGATCGCGCTTCTCGTTGGGG eGFP (SEQ ID TCTTTGCTCAGGGCGGACTGGGTGCTCAGGTAGTGGTTGTCGGG NO: 24) CAGCAGCACGGGGCCGTCGCCGATGGGGGTGTTCTGCTGGTAGT GGTCGGCGAGCTGCACGCTGCCGTCCTCGATGTTGTGGCGGATC TTGAAGTTCACCTTGATGCCGTTCTTCTGCTTGTCGGCCATGAT ATAGACGTTGTGGCTGTTGTAGTTGTACTCCAGCTTGTGCCCCA GGATGTTGCCGTCCTCCTTGAAGTCGATGCCCTTCAGCTCGATG CGGTTCACCAGGGTGTCGCCCTCGAACTTCACCTCGGCGCGGGT CTTGTAGTTGCCGTCGTCCTTGAAGAAGATGGTGCGCTCCTGGA CGTAGCCTTCGGGCATGGCGGACTTGAAGAAGTCGTGCTGCTTC ATGTGGTCGGGGTAGCGGCTGAAGCACTGCACGCCGTAGGTCAG GGTGGTCACGAGGGTGGGCCAGGGCACGGGCAGCTTGCCGGTGG TGCAGATGAACTTCAGGGTCAGCTTGCCGTAGGTGGCATCGCCC TCGCCCTCGCCGGACACGCTGAACTTGTGGCCGTTTACGTCGCC GTCCAGCTCGACCAGGATGGGCACCACCCCGGTGAACAGCTCCT CGCCCTTGCTCACCAT

TABLE 2 Plasmid Composition Plasmid Composition SEQUENCE IDENTIFIER (SEQ. ID. NO:)AND Elements SEQUENCE INFORMATION Plasmid TM017 Composition ΔITR  1 occurs at bp 4 through bp 106 of SEQ ID NO: 26 Human RLBP1  3 Promoter(short) Occurs at bp 119 through bp 708 of SEQ ID NO: 26 MODIFIED  4 SV40INTRON occurs at bp 723 through bp 905 of SEQ ID NO: 26 Added Kozak  5 occurs at bp 919 through bp 924 of SEQ ID NO: 26 HUMAN RLBP1  6 GENE CDS occurs at bp 925 through bp 1878 of SEQ ID NO: 26 SV40 POLYA  8 occurs at bp 1937 through bp 2172 of SEQ ID NO: 26 3′ ITR  9 occurs at bp 2201 through bp 2330 of SEQ ID NO: 26 AMP BACTERIAL 15 BACKBONE occurs at bp 2331 through bp 4949 of SEQ ID NO: 26 TM017 PLASMID 26 SEQUENCE ctgcgcgctcgctcgctcactgaggccgcccgggcaaagccc gggcgtcgggcgacctttggtcgcccggcctcagtgagcgag cgagcgcgcagagagggagtggggtaccacgcgtttgtcctc tccctgcttggccttaaccagccacatttctcaactgacccc actcactgcagaggtgaaaactaccatgccaggtcctgctgg ctgggggaggggtgggcaataggcctggatttgccagagctg ccactgtagatgtagtcatatttacgatttcccttcacctct tattaccctggtggtggtggtgggggggggggggtgctctct cagcaaccccaccccgggatcttgaggagaaagagggcagag aaaagagggaatgggactggcccagatcccagccccacagcc gggcttccacatggccgagcaggaactccagagcaggagcac acaaaggagggctttgatgcgcctccagccaggcccaggcct ctcccctctcccctttctctctgggtcttcctttgccccact gagggcctcctgtgagcccgatttaacggaaactgtgggcgg tgagaagttccttatgacacactaatcccaacctgctgaccg gaccacgcctccagcggagggaacctctagagctccaggaca ttcaggtaccaggtagccccaaggaggagctgccgaatcgat ggatcgggaactgaaaaaccagaaagttaactggtaagttta gtctttttgtcttttatttcaggtcccggatccggtggtggt gcaaatcaaagaactgctcctcagtggatgttgcctttactt ctaggcctgtacggaagtgttacttctgctctaaaagctgcg gaattgtacccgccccgggatccatcgattgaattcgccacc atgtcagaaggggtgggcacgttccgcatggtacctgaagag gaacaggagctccgtgcccaactggagcagctcacaaccaag gaccatggacctgtctttggcccgtgcagccagctgccccgc cacaccttgcagaaggccaaggatgagctgaacgagagagag gagacccgggaggaggcagtgcgagagctgcaggagatggtg caggcgcaggcggcctcgggggaggagctggcggtggccgtg gcggagagggtgcaagagaaggacagcggcttcttcctgcgc ttcatccgcgcacggaagttcaacgtgggccgtgcctatgag ctgctcagaggctatgtgaatttccggctgcagtaccctgag ctctttgacagcctgtccccagaggctgtccgctgcaccatt gaagctggctaccctggtgtcctctctagtcgggacaagtat ggccgagtggtcatgctcttcaacattgagaactggcaaagt caagaaatcacctttgatgagatcttgcaggcatattgcttc atcctggagaagctgctggagaatgaggaaactcaaatcaat ggcttctgcatcattgagaacttcaagggctttaccatgcag caggctgctagtctccggacttcagatctcaggaagatggtg gacatgctccaggattccttcccagcccggttcaaagccatc cacttcatccaccagccatggtacttcaccacgacctacaat gtggtcaagcccttcttgaagagcaagctgcttgagagggtc tttgtccacggggatgacctttctggtttctaccaggagatc gatgagaacatcctgccctctgacttcgggggcacgctgccc aagtatgatggcaaggccgttgctgagcagctctttggcccc caggcccaagctgagaacacagccttctgaggatcgtaccgg tcgacctgcagaagcttgcctcgagcagcgctgctcgagaga tctggatcataatcagccataccacatttgtagaggttttac ttgctttaaaaaacctcccacacctccccctgaacctgaaac ataaaatgaatgcaattgttgttgttaacttgtttattgcag cttataatggttacaaataaagcaatagcatcacaaatttca caaataaagcatttttttcactgcattctagttgtggtttgt ccaaactcatcaatgtatcttatcatgtctggtaaccacgtg cggaccgagcggccgcaggaacccctagtgatggagttggcc actccctctctgcgcgctcgctcgctcactgaggccgggcga ccaaaggtcgcccgacgcccgggctttgcccgggcggcctca gtgagcgagcgagcgcgcagctgcctgcaggggcgcctgatg cggtattttctccttacgcatctgtgcggtatttcacaccgc atacgtcaaagcaaccatagtacgcgccctgtagcggcgcat taagcgcggcgggtgtggtggttacgcgcagcgtgaccgcta cacttgccagcgccttagcgcccgctcctttcgctttcttcc cttcctttctcgccacgttcgccggctttccccgtcaagctc taaatcgggggctccctttagggttccgatttagtgctttac ggcacctcgaccccaaaaaacttgatttgggtgatggttcac gtagtgggccatcgccctgatagacggtttttcgccctttga cgttggagtccacgttctttaatagtggactcttgttccaaa ctggaacaacactcaactctatctcgggctattcttttgatt tataagggattttgccgatttcggtctattggttaaaaaatg agctgatttaacaaaaatttaacgcgaattttaacaaaatat taacgtttacaattttatggtgcactctcagtacaatctgct ctgatgccgcatagttaagccagccccgacacccgccaacac ccgctgacgcgccctgacgggcttgtctgctcccggcatccg cttacagacaagctgtgaccgtctccgggagctgcatgtgtc agaggttttcaccgtcatcaccgaaacgcgcgagacgaaagg gcctcgtgatacgcctatttttataggttaatgtcatgataa taatggtttcttagacgtcaggtggcacttttcggggaaatg tgcgcggaacccctatttgtttatttttctaaatacattcaa atatgtatccgctcatgagacaataaccctgataaatgcttc aataatattgaaaaaggaagagtatgagtattcaacatttcc gtgtcgcccttattcccttttttgcggcattttgccttcctg tttttgctcacccagaaacgctggtgaaagtaaaagatgctg aagatcagttgggtgcacgagtgggttacatcgaactggatc tcaacagcggtaagatccttgagagttttcgccccgaagaac gttttccaatgatgagcacttttaaagttctgctatgtggcg cggtattatcccgtattgacgccgggcaagagcaactcggtc gccgcatacactattctcagaatgacttggttgagtactcac cagtcacagaaaagcatcttacggatggcatgacagtaagag aattatgcagtgctgccataaccatgagtgataacactgcgg ccaacttacttctgacaacgatcggaggaccgaaggagctaa ccgcttttttgcacaacatgggggatcatgtaactcgccttg atcgttgggaaccggagctgaatgaagccataccaaacgacg agcgtgacaccacgatgcctgtagcaatggcaacaacgttgc gcaaactattaactggcgaactacttactctagcttcccggc aacaattaatagactggatggaggcggataaagttgcaggac cacttctgcgctcggcccttccggctggctggtttattgctg ataaatctggagccggtgagcgtgggtctcgcggtatcattg cagcactggggccagatggtaagccctcccgtatcgtagtta tctacacgacggggagtcaggcaactatggatgaacgaaata gacagatcgctgagataggtgcctcactgattaagcattggt aactgtcagaccaagtttactcatatatactttagattgatt taaaacttcatttttaatttaaaaggatctaggtgaagatcc tttttgataatctcatgaccaaaatcccttaacgtgagtttt cgttccactgagcgtcagaccccgtagaaaagatcaaaggat cttcttgaaatcctttttttctgcgcgtaatctgctgcttgc aaacaaaaaaaccaccgctaccagcggtggtttgtttgccgg atcaagagctaccaactctttttccgaaggtaactggcttca gcagagcgcagataccaaatactgttcttctagtgtagccgt agttaggccaccacttcaagaactctgtagcaccgcctacat acctcgctctgctaatcctgttaccagtggctgctgccagtg gcgataagtcgtgtcttaccgggttggactcaagacgatagt taccggataaggcgcagcggtcgggctgaacggggggttcgt gcacacagcccagcttggagcgaacgacctacaccgaactga gatacctacagcgtgagctatgagaaagcgccacgcttcccg aagggagaaaggcggacaggtatccggtaagcggcagggtcg gaacaggagagcgcacgagggagcttccagggggaaacgcct ggtatctttatagtcctgtcgggtttcgccacctctgacttg agcgtcgatttttgtgatgctcgtcaggggggcggagcctat ggaaaaacgccagcaacgcggcctttttacggttcctggcct tttgctggccttttgctcacatgtcctgcaggcag GENE CASSETTE 51 OF PLASMID cgcgctcgctcgctcactgaggccgcccgggcaaagcccggg TM017 OCCURS AT cgtcgggcgacctttggtcgcccggcctcagtgagcgagcga BP 4 THROUGH gcgcgcagagagggagtggggtaccacgcgtttgtcctctcc 2330 OF SEQ ID ctgcttggccttaaccagccacatttctcaactgaccccact NO: 26 cactgcagaggtgaaaactaccatgccaggtcctgctggctg ggggaggggtgggcaataggcctggatttgccagagctgcca ctgtagatgtagtcatatttacgatttcccttcacctcttat taccctggtggtggtggtgggggggggggggtgctctctcag caaccccaccccgggatcttgaggagaaagagggcagagaaa agagggaatgggactggcccagatcccagccccacagccggg cttccacatggccgagcaggaactccagagcaggagcacaca aaggagggctttgatgcgcctccagccaggcccaggcctctc ccctctcccctttctctctgggtcttcctttgccccactgag ggcctcctgtgagcccgatttaacggaaactgtgggcggtga gaagttccttatgacacactaatcccaacctgctgaccggac cacgcctccagcggagggaacctctagagctccaggacattc aggtaccaggtagccccaaggaggagctgccgaatcgatgga tcgggaactgaaaaaccagaaagttaactggtaagtttagtc tttttgtcttttatttcaggtcccggatccggtggtggtgca aatcaaagaactgctcctcagtggatgttgcctttacttcta ggcctgtacggaagtgttacttctgctctaaaagctgcggaa ttgtacccgccccgggatccatcgattgaattcgccaccatg tcagaaggggtgggcacgttccgcatggtacctgaagaggaa caggagctccgtgcccaactggagcagctcacaaccaaggac catggacctgtctttggcccgtgcagccagctgccccgccac accttgcagaaggccaaggatgagctgaacgagagagaggag acccgggaggaggcagtgcgagagctgcaggagatggtgcag gcgcaggcggcctcgggggaggagctggcggtggccgtggcg gagagggtgcaagagaaggacagcggcttcttcctgcgcttc atccgcgcacggaagttcaacgtgggccgtgcctatgagctg ctcagaggctatgtgaatttccggctgcagtaccctgagctc tttgacagcctgtccccagaggctgtccgctgcaccattgaa gctggctaccctggtgtcctctctagtcgggacaagtatggc cgagtggtcatgctcttcaacattgagaactggcaaagtcaa gaaatcacctttgatgagatcttgcaggcatattgcttcatc ctggagaagctgctggagaatgaggaaactcaaatcaatggc ttctgcatcattgagaacttcaagggctttaccatgcagcag gctgctagtctccggacttcagatctcaggaagatggtggac atgctccaggattccttcccagcccggttcaaagccatccac ttcatccaccagccatggtacttcaccacgacctacaatgtg gtcaagcccttcttgaagagcaagctgcttgagagggtcttt gtccacggggatgacctttctggtttctaccaggagatcgat gagaacatcctgccctctgacttcgggggcacgctgcccaag tatgatggcaaggccgttgctgagcagctctttggcccccag gcccaagctgagaacacagccttctgaggatcgtaccggtcg acctgcagaagcttgcctcgagcagcgctgctcgagagatct ggatcataatcagccataccacatttgtagaggttttacttg ctttaaaaaacctcccacacctccccctgaacctgaaacata aaatgaatgcaattgttgttgttaacttgtttattgcagctt ataatggttacaaataaagcaatagcatcacaaatttcacaa ataaagcatttttttcactgcattctagttgtggtttgtcca aactcatcaatgtatcttatcatgtctggtaaccacgtgcgg accgagcggccgcaggaacccctagtgatggagttggccact ccctctctgcgcgctcgctcgctcactgaggccgggcgacca aaggtcgcccgacgcccgggctttgcccgggcggcctcagtg agcgagcgagcgcgcag Plasmid TM037 Composition 5′ ITR  2 occurs @ bp 1 through bp 119 of SEQ ID NO: 27 Human RLBP1 10 Promoter(long) occurs @ bp 137 through bp 3293 of SEQ ID NO: 27 Added Kozak  5 occurs at bp 3300 through bp 3305 of SEQ ID NO: 27 HUMAN RLBP1  6 GENE CDS occurs at bp 3306 through bp 4259 of SEQ ID NO: 27 SV40 POLYA  8 occurs at bp 4318 through bp 4553 of SEQ ID NO: 27 3′ ITR  9 occurs at bp 4582 through bp 4711 of SEQ ID NO: 27 AMP BACTERIAL 15 BACKBONE occurs at bp 4712 through bp 7330 of SEQ ID NO: 27 Plasmid TM037 27 sequence CTGCGCGCTCGCTCGCTCACTGAGGCCGCCCGGGCGTCGGGC GACCTTTGGTCGCCCGGCCTCAGTGAGCGAGCGAGCGCGCAG AGAGGGAGTGGCCAACTCCATCACTAGGGGTTCCTGCGGCCG CACGCAGCTTTTGTCCTCTCCCTGCTTGGCCTTAACCAGCCA CATTTCTCAACTGACCCCACTCACTGCAGAGGTGAAAACTAC CATGCCAGGTCCTGCTGGCTGGGGGAGGGGTGGGCAATAGGC CTGGATTTGCCAGAGCTGCCACTGTAGATGTAGTCATATTTA CGATTTCCCTTCACCTCTTATTACCCTGGTGGTGGTGGTGGG GGGGGGGGGGTGCTCTCTCAGCAACCCCACCCCGGGATCTTG AGGAGAAAGAGGGCAGAGAAAAGAGGGAATGGGACTGGCCCA GATCCCAGCCCCACAGCCGGGCTTCCACATGGCCGAGCAGGA ACTCCAGAGCAGGAGCACACAAAGGAGGGCTTTGATGCGCCT CCAGCCAGGCCCAGGCCTCTCCCCTCTCCCCTTTCTCTCTGG GTCTTCCTTTGCCCCACTGAGGGCCTCCTGTGAGCCCGATTT AACGGAAACTGTGGGCGGTGAGAAGTTCCTTATGACACACTA ATCCCAACCTGCTGACCGGACCACGCCTCCAGCGGAGGGAAC CTCTAGAGCTCCAGGACATTCAGGTACCAGGTAGCCCCAAGG AGGAGCTGCCGACCTGGCAGGTAAGTCAATACCTGGGGCTTG CCTGGGCCAGGGAGCCCAGGACTGGGGTGAGGACTCAGGGGA GCAGGGAGACCACGTCCCAAGATGCCTGTAAAACTGAAACCA CCTGGCCATTCTCCAGGTTGAGCCAGACCAATTTGATGGCAG ATTTAGCAAATAAAAATACAGGACACCCAGTTAAATGTGAAT TTCAGATGAACAGCAAATACTTTTTTAGTATTAAAAAAGTTC ACATTTAGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCC GAGGCAGGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCC TGGCCAACATGGTGAAACCCCATCTCCACTAAAAATACCAAA AATTAGCCAGGCGTGCTGGTGGGCACCTGTAGTTCCAGCTAC TCAGGAGGCTAAGGCAGGAGAATTGCTTGAACCTGGGAGGCA GAGGTTGCAGTGAGCTGAGATCGCACCATTGCACTCTAGCCT GGGCGACAAGAACAAAACTCCATCTCAAAAAAAAAAAAAAAA AAAAAGTTCACATTTAACTGGGCATTCTGTATTTAATTGGTA ATCTGAGATGGCAGGGAACAGCATCAGCATGGTGTGAGGGAT AGGCATTTTTTCATTGTGTACAGCTTGTAAATCAGTATTTTT AAAACTCAAAGTTAATGGCTTGGGCATATTTAGAAAAGAGTT GCCGCACGGACTTGAACCCTGTATTCCTAAAATCTAGGATCT TGTTCTGATGGTCTGCACAACTGGCTGGGGGTGTCCAGCCAC TGTCCCTCTTGCCTGGGCTCCCCAGGGCAGTTCTGTCAGCCT CTCCATTTCCATTCCTGTTCCAGCAAAACCCAACTGATAGCA CAGCAGCATTTCAGCCTGTCTACCTCTGTGCCCACATACCTG GATGTCTACCAGCCAGAAAGGTGGCTTAGATTTGGTTCCTGT GGGTGGATTATGGCCCCCAGAACTTCCCTGTGCTTGCTGGGG GTGTGGAGTGGAAAGAGCAGGAAATGGGGGACCCTCCGATAC TCTATGGGGGTCCTCCAAGTCTCTTTGTGCAAGTTAGGGTAA TAATCAATATGGAGCTAAGAAAGAGAAGGGGAACTATGCTTT AGAACAGGACACTGTGCCAGGAGCATTGCAGAAATTATATGG TTTTCACGACAGTTCTTTTTGGTAGGTACTGTTATTATCCTC AGTTTGCAGATGAGGAAACTGAGACCCAGAAAGGTTAAATAA CTTGCTAGGGTCACACAAGTCATAACTGACAAAGCCTGATTC AAACCCAGGTCTCCCTAACCTTTAAGGTTTCTATGACGCCAG CTCTCCTAGGGAGTTTGTCTTCAGATGTCTTGGCTCTAGGTG TCAAAAAAAGACTTGGTGTCAGGCAGGCATAGGTTCAAGTCC CAACTCTGTCACTTACCAACTGTGACTAGGTGATTGAACTGA CCATGGAACCTGGTCACATGCAGGAGCAGGATGGTGAAGGGT TCTTGAAGGCACTTAGGCAGGACATTTAGGCAGGAGAGAAAA CCTGGAAACAGAAGAGCTGTCTCCAAAAATACCCACTGGGGA AGCAGGTTGTCATGTGGGCCATGAATGGGACCTGTTCTGGTA ACCAAGCATTGCTTATGTGTCCATTACATTTCATAACACTTC CATCCTACTTTACAGGGAACAACCAAGACTGGGGTTAAATCT CACAGCCTGCAAGTGGAAGAGAAGAACTTGAACCCAGGTCCA ACTTTTGCGCCACAGCAGGCTGCCTCTTGGTCCTGACAGGAA GTCACAACTTGGGTCTGAGTACTGATCCCTGGCTATTTTTTG GCTGTGTTACCTTGGACAAGTCACTTATTCCTCCTCCCGTTT CCTCCTATGTAAAATGGAAATAATAATGTTGACCCTGGGTCT GAGAGAGTGGATTTGAAAGTACTTAGTGCATCACAAAGCACA GAACACACTTCCAGTCTCGTGATTATGTACTTATGTAACTGG TCATCACCCATCTTGAGAATGAATGCATTGGGGAAAGGGCCA TCCACTAGGCTGCGAAGTTTCTGAGGGACTCCTTCGGGCTGG AGAAGGATGGCCACAGGAGGGAGGAGAGATTGCCTTATCCTG CAGTGATCATGTCATTGAGAACAGAGCCAGATTCTTTTTTTC CTGGCAGGGCCAACTTGTTTTAACATCTAAGGACTGAGCTAT TTGTGTCTGTGCCCTTTGTCCAAGCAGTGTTTCCCAAAGTGT AGCCCAAGAACCATCTCCCTCAGAGCCACCAGGAAGTGCTTT AAATTGCAGGTTCCTAGGCCACAGCCTGCACCTGCAGAGTCA GAATCATGGAGGTTGGGACCCAGGCACCTGCGTTTCTAACAA ATGCCTCGGGTGATTCTGATGCAATTGAAAGTTTGAGATCCA CAGTTCTGAGACAATAACAGAATGGTTTTTCTAACCCCTGCA GCCCTGACTTCCTATCCTAGGGAAGGGGCCGGCTGGAGAGGC CAGGACAGAGAAAGCAGATCCCTTCTTTTTCCAAGGACTCTG TGTCTTCCATAGGCAACGAATTCGCCACCATGTCAGAAGGGG TGGGCACGTTCCGCATGGTACCTGAAGAGGAACAGGAGCTCC GTGCCCAACTGGAGCAGCTCACAACCAAGGACCATGGACCTG TCTTTGGCCCGTGCAGCCAGCTGCCCCGCCACACCTTGCAGA AGGCCAAGGATGAGCTGAACGAGAGAGAGGAGACCCGGGAGG AGGCAGTGCGAGAGCTGCAGGAGATGGTGCAGGCGCAGGCGG CCTCGGGGGAGGAGCTGGCGGTGGCCGTGGCGGAGAGGGTGC AAGAGAAGGACAGCGGCTTCTTCCTGCGCTTCATCCGCGCAC GGAAGTTCAACGTGGGCCGTGCCTATGAGCTGCTCAGAGGCT ATGTGAATTTCCGGCTGCAGTACCCTGAGCTCTTTGACAGCC TGTCCCCAGAGGCTGTCCGCTGCACCATTGAAGCTGGCTACC CTGGTGTCCTCTCTAGTCGGGACAAGTATGGCCGAGTGGTCA TGCTCTTCAACATTGAGAACTGGCAAAGTCAAGAAATCACCT TTGATGAGATCTTGCAGGCATATTGCTTCATCCTGGAGAAGC TGCTGGAGAATGAGGAAACTCAAATCAATGGCTTCTGCATCA TTGAGAACTTCAAGGGCTTTACCATGCAGCAGGCTGCTAGTC TCCGGACTTCAGATCTCAGGAAGATGGTGGACATGCTCCAGG ATTCCTTCCCAGCCCGGTTCAAAGCCATCCACTTCATCCACC AGCCATGGTACTTCACCACGACCTACAATGTGGTCAAGCCCT TCTTGAAGAGCAAGCTGCTTGAGAGGGTCTTTGTCCACGGGG ATGACCTTTCTGGTTTCTACCAGGAGATCGATGAGAACATCC TGCCCTCTGACTTCGGGGGCACGCTGCCCAAGTATGATGGCA AGGCCGTTGCTGAGCAGCTCTTTGGCCCCCAGGCCCAAGCTG AGAACACAGCCTTCTGAGGATCGTACCGGTCGACCTGCAGAA GCTTGCCTCGAGCAGCGCTGCTCGAGAGATCTGGATCATAAT CAGCCATACCACATTTGTAGAGGTTTTACTTGCTTTAAAAAA CCTCCCACACCTCCCCCTGAACCTGAAACATAAAATGAATGC AATTGTTGTTGTTAACTTGTTTATTGCAGCTTATAATGGTTA CAAATAAAGCAATAGCATCACAAATTTCACAAATAAAGCATT TTTTTCACTGCATTCTAGTTGTGGTTTGTCCAAACTCATCAA TGTATCTTATCATGTCTGGTAACCACGTGCGGACCGAGCGGC CGCAGGAACCCCTAGTGATGGAGTTGGCCACTCCCTCTCTGC GCGCTCGCTCGCTCACTGAGGCCGGGCGACCAAAGGTCGCCC GACGCCCGGGCTTTGCCCGGGCGGCCTCAGTGAGCGAGCGAG CGCGCAGCTGCCTGCAGGGGCGCCTGATGCGGTATTTTCTCC TTACGCATCTGTGCGGTATTTCACACCGCATACGTCAAAGCA ACCATAGTACGCGCCCTGTAGCGGCGCATTAAGCGCGGCGGG TGTGGTGGTTACGCGCAGCGTGACCGCTACACTTGCCAGCGC CTTAGCGCCCGCTCCTTTCGCTTTCTTCCCTTCCTTTCTCGC CACGTTCGCCGGCTTTCCCCGTCAAGCTCTAAATCGGGGGCT CCCTTTAGGGTTCCGATTTAGTGCTTTACGGCACCTCGACCC CAAAAAACTTGATTTGGGTGATGGTTCACGTAGTGGGCCATC GCCCTGATAGACGGTTTTTCGCCCTTTGACGTTGGAGTCCAC GTTCTTTAATAGTGGACTCTTGTTCCAAACTGGAACAACACT CAACTCTATCTCGGGCTATTCTTTTGATTTATAAGGGATTTT GCCGATTTCGGTCTATTGGTTAAAAAATGAGCTGATTTAACA AAAATTTAACGCGAATTTTAACAAAATATTAACGTTTACAAT TTTATGGTGCACTCTCAGTACAATCTGCTCTGATGCCGCATA GTTAAGCCAGCCCCGACACCCGCCAACACCCGCTGACGCGCC CTGACGGGCTTGTCTGCTCCCGGCATCCGCTTACAGACAAGC TGTGACCGTCTCCGGGAGCTGCATGTGTCAGAGGTTTTCACC GTCATCACCGAAACGCGCGAGACGAAAGGGCCTCGTGATACG CCTATTTTTATAGGTTAATGTCATGATAATAATGGTTTCTTA GACGTCAGGTGGCACTTTTCGGGGAAATGTGCGCGGAACCCC TATTTGTTTATTTTTCTAAATACATTCAAATATGTATCCGCT CATGAGACAATAACCCTGATAAATGCTTCAATAATATTGAAA AAGGAAGAGTATGAGTATTCAACATTTCCGTGTCGCCCTTAT TCCCTTTTTTGCGGCATTTTGCCTTCCTGTTTTTGCTCACCC AGAAACGCTGGTGAAAGTAAAAGATGCTGAAGATCAGTTGGG TGCACGAGTGGGTTACATCGAACTGGATCTCAACAGCGGTAA GATCCTTGAGAGTTTTCGCCCCGAAGAACGTTTTCCAATGAT GAGCACTTTTAAAGTTCTGCTATGTGGCGCGGTATTATCCCG TATTGACGCCGGGCAAGAGCAACTCGGTCGCCGCATACACTA TTCTCAGAATGACTTGGTTGAGTACTCACCAGTCACAGAAAA GCATCTTACGGATGGCATGACAGTAAGAGAATTATGCAGTGC TGCCATAACCATGAGTGATAACACTGCGGCCAACTTACTTCT GACAACGATCGGAGGACCGAAGGAGCTAACCGCTTTTTTGCA CAACATGGGGGATCATGTAACTCGCCTTGATCGTTGGGAACC GGAGCTGAATGAAGCCATACCAAACGACGAGCGTGACACCAC GATGCCTGTAGCAATGGCAACAACGTTGCGCAAACTATTAAC TGGCGAACTACTTACTCTAGCTTCCCGGCAACAATTAATAGA CTGGATGGAGGCGGATAAAGTTGCAGGACCACTTCTGCGCTC GGCCCTTCCGGCTGGCTGGTTTATTGCTGATAAATCTGGAGC CGGTGAGCGTGGGTCTCGCGGTATCATTGCAGCACTGGGGCC AGATGGTAAGCCCTCCCGTATCGTAGTTATCTACACGACGGG GAGTCAGGCAACTATGGATGAACGAAATAGACAGATCGCTGA GATAGGTGCCTCACTGATTAAGCATTGGTAACTGTCAGACCA AGTTTACTCATATATACTTTAGATTGATTTAAAACTTCATTT TTAATTTAAAAGGATCTAGGTGAAGATCCTTTTTGATAATCT CATGACCAAAATCCCTTAACGTGAGTTTTCGTTCCACTGAGC GTCAGACCCCGTAGAAAAGATCAAAGGATCTTCTTGAAATCC TTTTTTTCTGCGCGTAATCTGCTGCTTGCAAACAAAAAAACC ACCGCTACCAGCGGTGGTTTGTTTGCCGGATCAAGAGCTACC AACTCTTTTTCCGAAGGTAACTGGCTTCAGCAGAGCGCAGAT ACCAAATACTGTTCTTCTAGTGTAGCCGTAGTTAGGCCACCA CTTCAAGAACTCTGTAGCACCGCCTACATACCTCGCTCTGCT AATCCTGTTACCAGTGGCTGCTGCCAGTGGCGATAAGTCGTG TCTTACCGGGTTGGACTCAAGACGATAGTTACCGGATAAGGC GCAGCGGTCGGGCTGAACGGGGGGTTCGTGCACACAGCCCAG CTTGGAGCGAACGACCTACACCGAACTGAGATACCTACAGCG TGAGCTATGAGAAAGCGCCACGCTTCCCGAAGGGAGAAAGGC GGACAGGTATCCGGTAAGCGGCAGGGTCGGAACAGGAGAGCG CACGAGGGAGCTTCCAGGGGGAAACGCCTGGTATCTTTATAG TCCTGTCGGGTTTCGCCACCTCTGACTTGAGCGTCGATTTTT GTGATGCTCGTCAGGGGGGCGGAGCCTATGGAAAAACGCCAG CAACGCGGCCTTTTTACGGTTCCTGGCCTTTTGCTGGCCTTT TGCTCACATGTCCTGCAGGCAG GENE CASSETTE 52 OF PLASMID ctgcgcgctcgctcgctcactgaggccgcccgggcgtcgggc TM037 OCCURS AT gacctttggtcgcccggcctcagtgagcgagcgagcgcgcag BP 1 THROUGH agagggagtggccaactccatcactaggggttcctgcggccg 4711 OF SEQ ID cacgcagcttttgtcctctccctgcttggccttaaccagcca NO: 27 catttctcaactgaccccactcactgcagaggtgaaaactac catgccaggtcctgctggctgggggaggggtgggcaataggc ctggatttgccagagctgccactgtagatgtagtcatattta cgatttcccttcacctcttattaccctggtggtggtggtggg ggggggggggtgctctctcagcaaccccaccccgggatcttg aggagaaagagggcagagaaaagagggaatgggactggccca gatcccagccccacagccgggcttccacatggccgagcagga actccagagcaggagcacacaaaggagggctttgatgcgcct ccagccaggcccaggcctctcccctctcccctttctctctgg gtcttcctttgccccactgagggcctcctgtgagcccgattt aacggaaactgtgggcggtgagaagttccttatgacacacta atcccaacctgctgaccggaccacgcctccagcggagggaac ctctagagctccaggacattcaggtaccaggtagccccaagg aggagctgccgacctggcaggtaagtcaatacctggggcttg cctgggccagggagcccaggactggggtgaggactcagggga gcagggagaccacgtcccaagatgcctgtaaaactgaaacca cctggccattctccaggttgagccagaccaatttgatggcag atttagcaaataaaaatacaggacacccagttaaatgtgaat ttcagatgaacagcaaatacttttttagtattaaaaaagttc acatttaggctcacgcctgtaatcccagcactttgggaggcc gaggcaggcagatcacctgaggtcaggagttcgagaccagcc tggccaacatggtgaaaccccatctccactaaaaataccaaa aattagccaggcgtgctggtgggcacctgtagttccagctac tcaggaggctaaggcaggagaattgcttgaacctgggaggca gaggttgcagtgagctgagatcgcaccattgcactctagcct gggcgacaagaacaaaactccatctcaaaaaaaaaaaaaaaa aaaaagttcacatttaactgggcattctgtatttaattggta atctgagatggcagggaacagcatcagcatggtgtgagggat aggcattttttcattgtgtacagcttgtaaatcagtattttt aaaactcaaagttaatggcttgggcatatttagaaaagagtt gccgcacggacttgaaccctgtattcctaaaatctaggatct tgttctgatggtctgcacaactggctgggggtgtccagccac tgtccctcttgcctgggctccccagggcagttctgtcagcct ctccatttccattcctgttccagcaaaacccaactgatagca cagcagcatttcagcctgtctacctctgtgcccacatacctg gatgtctaccagccagaaaggtggcttagatttggttcctgt gggtggattatggcccccagaacttccctgtgcttgctgggg gtgtggagtggaaagagcaggaaatgggggaccctccgatac tctatgggggtcctccaagtctctttgtgcaagttagggtaa taatcaatatggagctaagaaagagaaggggaactatgcttt agaacaggacactgtgccaggagcattgcagaaattatatgg ttttcacgacagttctttttggtaggtactgttattatcctc agtttgcagatgaggaaactgagacccagaaaggttaaataa cttgctagggtcacacaagtcataactgacaaagcctgattc aaacccaggtctccctaacctttaaggtttctatgacgccag ctctcctagggagtttgtcttcagatgtcttggctctaggtg tcaaaaaaagacttggtgtcaggcaggcataggttcaagtcc caactctgtcacttaccaactgtgactaggtgattgaactga ccatggaacctggtcacatgcaggagcaggatggtgaagggt tcttgaaggcacttaggcaggacatttaggcaggagagaaaa cctggaaacagaagagctgtctccaaaaatacccactgggga agcaggttgtcatgtgggccatgaatgggacctgttctggta accaagcattgcttatgtgtccattacatttcataacacttc catcctactttacagggaacaaccaagactggggttaaatct cacagcctgcaagtggaagagaagaacttgaacccaggtcca acttttgcgccacagcaggctgcctcttggtcctgacaggaa gtcacaacttgggtctgagtactgatccctggctattttttg gctgtgttaccttggacaagtcacttattcctcctcccgttt cctcctatgtaaaatggaaataataatgttgaccctgggtct gagagagtggatttgaaagtacttagtgcatcacaaagcaca gaacacacttccagtctcgtgattatgtacttatgtaactgg tcatcacccatcttgagaatgaatgcattggggaaagggcca tccactaggctgcgaagtttctgagggactccttcgggctgg agaaggatggccacaggagggaggagagattgccttatcctg cagtgatcatgtcattgagaacagagccagattctttttttc ctggcagggccaacttgttttaacatctaaggactgagctat ttgtgtctgtgccctttgtccaagcagtgtttcccaaagtgt agcccaagaaccatctccctcagagccaccaggaagtgcttt aaattgcaggttcctaggccacagcctgcacctgcagagtca gaatcatggaggttgggacccaggcacctgcgtttctaacaa atgcctcgggtgattctgatgcaattgaaagtttgagatcca cagttctgagacaataacagaatggtttttctaacccctgca gccctgacttcctatcctagggaaggggccggctggagaggc caggacagagaaagcagatcccttctttttccaaggactctg tgtcttccataggcaacgaattcgccaccatgtcagaagggg tgggcacgttccgcatggtacctgaagaggaacaggagctcc gtgcccaactggagcagctcacaaccaaggaccatggacctg tctttggcccgtgcagccagctgccccgccacaccttgcaga aggccaaggatgagctgaacgagagagaggagacccgggagg aggcagtgcgagagctgcaggagatggtgcaggcgcaggcgg cctcgggggaggagctggcggtggccgtggcggagagggtgc aagagaaggacagcggcttcttcctgcgcttcatccgcgcac ggaagttcaacgtgggccgtgcctatgagctgctcagaggct atgtgaatttccggctgcagtaccctgagctctttgacagcc tgtccccagaggctgtccgctgcaccattgaagctggctacc ctggtgtcctctctagtcgggacaagtatggccgagtggtca tgctcttcaacattgagaactggcaaagtcaagaaatcacct ttgatgagatcttgcaggcatattgcttcatcctggagaagc tgctggagaatgaggaaactcaaatcaatggcttctgcatca ttgagaacttcaagggctttaccatgcagcaggctgctagtc tccggacttcagatctcaggaagatggtggacatgctccagg attccttcccagcccggttcaaagccatccacttcatccacc agccatggtacttcaccacgacctacaatgtggtcaagccct tcttgaagagcaagctgcttgagagggtctttgtccacgggg atgacctttctggtttctaccaggagatcgatgagaacatcc tgccctctgacttcgggggcacgctgcccaagtatgatggca aggccgttgctgagcagctctttggcccccaggcccaagctg agaacacagccttctgaggatcgtaccggtcgacctgcagaa gcttgcctcgagcagcgctgctcgagagatctggatcataat cagccataccacatttgtagaggttttacttgctttaaaaaa cctcccacacctccccctgaacctgaaacataaaatgaatgc aattgttgttgttaacttgtttattgcagcttataatggtta caaataaagcaatagcatcacaaatttcacaaataaagcatt tttttcactgcattctagttgtggtttgtccaaactcatcaa tgtatcttatcatgtctggtaaccacgtgcggaccgagcggc cgcaggaacccctagtgatggagttggccactccctctctgc gcgctcgctcgctcactgaggccgggcgaccaaaggtcgccc gacgcccgggctttgcccgggcggcctcagtgagcgagcgag cgcgcag Plasmid AG007 Composition 5′ ITR  2 occurs @ bp 1 through bp 119 of SEQ ID NO: 28 Human RPE65 11 Promoter occurs @ bp 134 through bp 1718 of SEQ ID NO: 28 ADDED-KOZAK  5 occurs @ bp 1725 through bp 1730 of SEQ ID NO: 28 HUMAN RLBP1  6 GENE CDS occurs at bp 1731 through bp 2684 of SEQ ID NO: 28 SV40 POLYA  8 occurs at bp 2742 through bp 2977 of SEQ ID NO: 28 RLBP1 INTRONIC 14 SEQUENCE AS occurs at bp 2985 through bp 4487 of SEQ STUFFER ID NO: 28 SEQUENCE 3′ ITR  9 occurs at bp 4516 through bp 4645 of SEQ ID NO: 28 AMP BACTERIAL 15 BACKBONE occurs at bp 4646 through bp 7264 of SEQ ID NO: 28 AG007 Plasmid 28 Sequence ctgcgcgctcgctcgctcactgaggccgcccgggcgtcgggc gacctttggtcgcccggcctcagtgagcgagcgagcgcgcag agagggagtggccaactccatcactaggggttcctgcggccg cacgcgttacgtaatatttattgaagtttaatattgtgtttg tgatacagaagtatttgctttaattctaaataaaaattttat gcttttattgctggtttaagaagatttggattatccttgtac tttgaggagaagtttcttatttgaaatattttggaaacaggt cttttaatgtggaaagatagatattaatctcctcttctatta ctctccaagatccaacaaaagtgattataccccccaaaatat gatggtagtatcttatactaccatcattttataggcataggg ctcttagctgcaaataatggaactaactctaataaagcagaa cgcaaatattgtaaatattagagagctaacaatctctgggat ggctaaaggatggagcttggaggctacccagccagtaacaat attccgggctccactgttgaatggagacactacaactgcctt ggatgggcagagatattatggatgctaagccccaggtgctac cattaggacttctaccactgtccctaacgggtggagcccatc acatgcctatgccctcactgtaaggaaatgaagctactgttg tatatcttgggaagcacttggattaattgttatacagttttg ttgaagaagacccctagggtaagtagccataactgcacacta aatttaaaattgttaatgagtttctcaaaaaaaatgttaagg ttgttagctggtatagtatatatcttgcctgttttccaagga cttctttgggcagtaccttgtctgtgctggcaagcaactgag acttaatgaaagagtattggagatatgaatgaattgatgctg tatactctcagagtgccaaacatataccaatggacaagaagg tgaggcagagagcagacaggcattagtgacaagcaaagatat gcagaatttcattctcagcaaatcaaaagtcctcaacctggt tggaagaatattggcactgaatggtatcaataaggttgctag agagggttagaggtgcacaatgtgcttccataacattttata cttctccaatcttagcactaatcaaacatggttgaatacttt gtttactataactcttacagagttataagatctgtgaagaca gggacagggacaatacccatctctgtctggttcataggtggt atgtaatagatatttttaaaaataagtgagttaatgaatgag ggtgagaatgaaggcacagaggtattagggggaggtgggccc cagagaatggtgccaaggtccagtggggtgactgggatcagc tcaggcctgacgctggccactcccacctagctcctttctttc taatctgttctcattctccttgggaaggattgaggtctctgg aaaacagccaaacaactgttatgggaacagcaagcccaaata aagccaagcatcagggggatctgagagctgaaagcaacttct gttccccctccctcagctgaaggggtggggaagggctcccaa agccataactccttttaagggatttagaaggcataaaaaggc ccctggctgagaacttccttcttcattctgcagttggtgaat tcgccaccatgtcagaaggggtgggcacgttccgcatggtac ctgaagaggaacaggagctccgtgcccaactggagcagctca caaccaaggaccatggacctgtctttggcccgtgcagccagc tgccccgccacaccttgcagaaggccaaggatgagctgaacg agagagaggagacccgggaggaggcagtgcgagagctgcagg agatggtgcaggcgcaggcggcctcgggggaggagctggcgg tggccgtggcggagagggtgcaagagaaggacagcggcttct tcctgcgcttcatccgcgcacggaagttcaacgtgggccgtg cctatgagctgctcagaggctatgtgaatttccggctgcagt accctgagctctttgacagcctgtccccagaggctgtccgct gcaccattgaagctggctaccctggtgtcctctctagtcggg acaagtatggccgagtggtcatgctcttcaacattgagaact ggcaaagtcaagaaatcacctttgatgagatcttgcaggcat attgcttcatcctggagaagctgctggagaatgaggaaactc aaatcaatggcttctgcatcattgagaacttcaagggcttta ccatgcagcaggctgctagtctccggacttcagatctcagga agatggtggacatgctccaggattccttcccagcccggttca aagccatccacttcatccaccagccatggtacttcaccacga cctacaatgtggtcaagcccttcttgaagagcaagctgcttg agagggtctttgtccacggggatgacctttctggtttctacc aggagatcgatgagaacatcctgccctctgacttcgggggca cgctgcccaagtatgatggcaaggccgttgctgagcagctct ttggcccccaggcccaagctgagaacacagccttctgaggat ctaccggtcgacctgcagaagcttgcctcgagcagcgctgct cgagagatctggatcataatcagccataccacatttgtagag gttttacttgctttaaaaaacctcccacacctccccctgaac ctgaaacataaaatgaatgcaattgttgttgttaacttgttt attgcagcttataatggttacaaataaagcaatagcatcaca aatttcacaaataaagcatttttttcactgcattctagttgt ggtttgtccaaactcatcaatgtatcttatcatgtctggtaa ccattctccaggttgagccagaccaatttgatggtagattta gcaaataaaaatacaggacacccagttaaatgtgaatttccg atgaacagcaaatacttttttagtattaaaaaagttcacatt taggctcacgcctgtaatcccagcactttgggaggccgaggc aggcagatcacctgaggtcaggagttcgagaccagcctggcc aacatggtgaaaccccatctccactaaaaataccaaaaatta gccaggcgtgctggtgggcacctgtagttccagctactcagg aggctaaggcaggagaattgcttgaacctgggaggcagaggt tgcagtgagctgagatcgcaccattgcactctagcctgggcg acaagaacaaaactccatctcaaaaaaaaaaaaaaaaaaaaa gttcacatttaactgggcattctgtatttaattggtaatctg agatggcagggaacagcatcagcatggtgtgagggataggca ttttttcattgtgtacagcttgtaaatcagtatttttaaaac tcaaagttaatggcttgggcatatttagaaaagagttgccgc acggacttgaaccctgtattcctaaaatctaggatcttgttc tgatggtctgcacaactggctgggggtgtccagccactgtcc ctcttgcctgggctccccagggcagttctgtcagcctctcca tttccattcctgttccagcaaaacccaactgatagcacagca gcatttcagcctgtctacctctgtgcccacatacctggatgt ctaccagccagaaaggtggcttagatttggttcctgtgggtg gattatggcccccagaacttccctgtgcttgctgggggtgtg gagtggaaagagcaggaaatgggggaccctccgatactctat gggggtcctccaagtctctttgtgcaagttagggtaataatc aatatggagctaagaaagagaaggggaactatgctttagaac aggacactgtgccaggagcattgcagaaattatatggttttc acgacagttctttttggtaggtactgttattatcctcagttt gcagatgaggaaactgagacccagaaaggttaaataacttgc tagggtcacacaagtcataactgacaaagcctgattcaaacc caggtctccctaacctttaaggtttctatgacgccagctctc ctagggagtttgtcttcagatgtcttggctctaggtgtcaaa aaaagacttggtgtcaggcaggcataggttcaagtcccaact ctgtcacttaccaactgtgactaggtgattgaactgaccatg gaacctggtcacatgcaggagcaggatggtgaagggttcttg aaggcacttaggcaggacatttaggcaggagagaaaacctgg aaacagaagagctgtctccaaaaatacccactggggaagcag gttgtcatgtgggccatgaatgggacctgttctggggtaacc acgtgcggaccgagcggccgcaggaacccctagtgatggagt tggccactccctctctgcgcgctcgctcgctcactgaggccg ggcgaccaaaggtcgcccgacgcccgggctttgcccgggcgg cctcagtgagcgagcgagcgcgcagctgcctgcaggggcgcc tgatgcggtattttctccttacgcatctgtgcggtatttcac accgcatacgtcaaagcaaccatagtacgcgccctgtagcgg cgcattaagcgcggcgggtgtggtggttacgcgcagcgtgac cgctacacttgccagcgccttagcgcccgctcctttcgcttt cttcccttcctttctcgccacgttcgccggctttccccgtca agctctaaatcgggggctccctttagggttccgatttagtgc tttacggcacctcgaccccaaaaaacttgatttgggtgatgg ttcacgtagtgggccatcgccctgatagacggtttttcgccc tttgacgttggagtccacgttctttaatagtggactcttgtt ccaaactggaacaacactcaactctatctcgggctattcttt tgatttataagggattttgccgatttcggtctattggttaaa aaatgagctgatttaacaaaaatttaacgcgaattttaacaa aatattaacgtttacaattttatggtgcactctcagtacaat ctgctctgatgccgcatagttaagccagccccgacacccgcc aacacccgctgacgcgccctgacgggcttgtctgctcccggc atccgcttacagacaagctgtgaccgtctccgggagctgcat gtgtcagaggttttcaccgtcatcaccgaaacgcgcgagacg aaagggcctcgtgatacgcctatttttataggttaatgtcat gataataatggtttcttagacgtcaggtggcacttttcgggg aaatgtgcgcggaacccctatttgtttatttttctaaataca ttcaaatatgtatccgctcatgagacaataaccctgataaat gcttcaataatattgaaaaaggaagagtatgagtattcaaca tttccgtgtcgcccttattcccttttttgcggcattttgcct tcctgtttttgctcacccagaaacgctggtgaaagtaaaaga tgctgaagatcagttgggtgcacgagtgggttacatcgaact ggatctcaacagcggtaagatccttgagagttttcgccccga agaacgttttccaatgatgagcacttttaaagttctgctatg tggcgcggtattatcccgtattgacgccgggcaagagcaact cggtcgccgcatacactattctcagaatgacttggttgagta ctcaccagtcacagaaaagcatcttacggatggcatgacagt aagagaattatgcagtgctgccataaccatgagtgataacac tgcggccaacttacttctgacaacgatcggaggaccgaagga gctaaccgcttttttgcacaacatgggggatcatgtaactcg ccttgatcgttgggaaccggagctgaatgaagccataccaaa cgacgagcgtgacaccacgatgcctgtagcaatggcaacaac gttgcgcaaactattaactggcgaactacttactctagcttc ccggcaacaattaatagactggatggaggcggataaagttgc aggaccacttctgcgctcggcccttccggctggctggtttat tgctgataaatctggagccggtgagcgtgggtctcgcggtat cattgcagcactggggccagatggtaagccctcccgtatcgt agttatctacacgacggggagtcaggcaactatggatgaacg aaatagacagatcgctgagataggtgcctcactgattaagca ttggtaactgtcagaccaagtttactcatatatactttagat tgatttaaaacttcatttttaatttaaaaggatctaggtgaa gatcctttttgataatctcatgaccaaaatcccttaacgtga gttttcgttccactgagcgtcagaccccgtagaaaagatcaa aggatcttcttgaaatcctttttttctgcgcgtaatctgctg cttgcaaacaaaaaaaccaccgctaccagcggtggtttgttt gccggatcaagagctaccaactctttttccgaaggtaactgg cttcagcagagcgcagataccaaatactgttcttctagtgta gccgtagttaggccaccacttcaagaactctgtagcaccgcc tacatacctcgctctgctaatcctgttaccagtggctgctgc cagtggcgataagtcgtgtcttaccgggttggactcaagacg atagttaccggataaggcgcagcggtcgggctgaacgggggg ttcgtgcacacagcccagcttggagcgaacgacctacaccga actgagatacctacagcgtgagctatgagaaagcgccacgct tcccgaagggagaaaggcggacaggtatccggtaagcggcag ggtcggaacaggagagcgcacgagggagcttccagggggaaa cgcctggtatctttatagtcctgtcgggtttcgccacctctg acttgagcgtcgatttttgtgatgctcgtcaggggggcggag cctatggaaaaacgccagcaacgcggcctttttacggttcct ggccttttgctggccttttgctcacatgtcctgcaggcag GENE CASSETTE 53 OF PLASMID ctgcgcgctcgctcgctcactgaggccgcccgggcgtcgggc AG007 OCCURS AT gacctttggtcgcccggcctcagtgagcgagcgagcgcgcag BP 1 THROUGH agagggagtggccaactccatcactaggggttcctgcggccg 4645 OF SEQ ID cacgcgttacgtaatatttattgaagtttaatattgtgtttg NO: 28 tgatacagaagtatttgctttaattctaaataaaaattttat gcttttattgctggtttaagaagatttggattatccttgtac tttgaggagaagtttcttatttgaaatattttggaaacaggt cttttaatgtggaaagatagatattaatctcctcttctatta ctctccaagatccaacaaaagtgattataccccccaaaatat gatggtagtatcttatactaccatcattttataggcataggg ctcttagctgcaaataatggaactaactctaataaagcagaa cgcaaatattgtaaatattagagagctaacaatctctgggat ggctaaaggatggagcttggaggctacccagccagtaacaat attccgggctccactgttgaatggagacactacaactgcctt ggatgggcagagatattatggatgctaagccccaggtgctac cattaggacttctaccactgtccctaacgggtggagcccatc acatgcctatgccctcactgtaaggaaatgaagctactgttg tatatcttgggaagcacttggattaattgttatacagttttg ttgaagaagacccctagggtaagtagccataactgcacacta aatttaaaattgttaatgagtttctcaaaaaaaatgttaagg ttgttagctggtatagtatatatcttgcctgttttccaagga cttctttgggcagtaccttgtctgtgctggcaagcaactgag acttaatgaaagagtattggagatatgaatgaattgatgctg tatactctcagagtgccaaacatataccaatggacaagaagg tgaggcagagagcagacaggcattagtgacaagcaaagatat gcagaatttcattctcagcaaatcaaaagtcctcaacctggt tggaagaatattggcactgaatggtatcaataaggttgctag agagggttagaggtgcacaatgtgcttccataacattttata cttctccaatcttagcactaatcaaacatggttgaatacttt gtttactataactcttacagagttataagatctgtgaagaca gggacagggacaatacccatctctgtctggttcataggtggt atgtaatagatatttttaaaaataagtgagttaatgaatgag ggtgagaatgaaggcacagaggtattagggggaggtgggccc cagagaatggtgccaaggtccagtggggtgactgggatcagc tcaggcctgacgctggccactcccacctagctcctttctttc taatctgttctcattctccttgggaaggattgaggtctctgg aaaacagccaaacaactgttatgggaacagcaagcccaaata aagccaagcatcagggggatctgagagctgaaagcaacttct gttccccctccctcagctgaaggggtggggaagggctcccaa agccataactccttttaagggatttagaaggcataaaaaggc ccctggctgagaacttccttcttcattctgcagttggtgaat tcgccaccatgtcagaaggggtgggcacgttccgcatggtac ctgaagaggaacaggagctccgtgcccaactggagcagctca caaccaaggaccatggacctgtctttggcccgtgcagccagc tgccccgccacaccttgcagaaggccaaggatgagctgaacg agagagaggagacccgggaggaggcagtgcgagagctgcagg agatggtgcaggcgcaggcggcctcgggggaggagctggcgg tggccgtggcggagagggtgcaagagaaggacagcggcttct tcctgcgcttcatccgcgcacggaagttcaacgtgggccgtg cctatgagctgctcagaggctatgtgaatttccggctgcagt accctgagctctttgacagcctgtccccagaggctgtccgct gcaccattgaagctggctaccctggtgtcctctctagtcggg acaagtatggccgagtggtcatgctcttcaacattgagaact ggcaaagtcaagaaatcacctttgatgagatcttgcaggcat attgcttcatcctggagaagctgctggagaatgaggaaactc aaatcaatggcttctgcatcattgagaacttcaagggcttta ccatgcagcaggctgctagtctccggacttcagatctcagga agatggtggacatgctccaggattccttcccagcccggttca aagccatccacttcatccaccagccatggtacttcaccacga cctacaatgtggtcaagcccttcttgaagagcaagctgcttg agagggtctttgtccacggggatgacctttctggtttctacc aggagatcgatgagaacatcctgccctctgacttcgggggca cgctgcccaagtatgatggcaaggccgttgctgagcagctct ttggcccccaggcccaagctgagaacacagccttctgaggat ctaccggtcgacctgcagaagcttgcctcgagcagcgctgct cgagagatctggatcataatcagccataccacatttgtagag gttttacttgctttaaaaaacctcccacacctccccctgaac ctgaaacataaaatgaatgcaattgttgttgttaacttgttt attgcagcttataatggttacaaataaagcaatagcatcaca aatttcacaaataaagcatttttttcactgcattctagttgt ggtttgtccaaactcatcaatgtatcttatcatgtctggtaa ccattctccaggttgagccagaccaatttgatggtagattta gcaaataaaaatacaggacacccagttaaatgtgaatttccg atgaacagcaaatacttttttagtattaaaaaagttcacatt taggctcacgcctgtaatcccagcactttgggaggccgaggc aggcagatcacctgaggtcaggagttcgagaccagcctggcc aacatggtgaaaccccatctccactaaaaataccaaaaatta gccaggcgtgctggtgggcacctgtagttccagctactcagg aggctaaggcaggagaattgcttgaacctgggaggcagaggt tgcagtgagctgagatcgcaccattgcactctagcctgggcg acaagaacaaaactccatctcaaaaaaaaaaaaaaaaaaaaa gttcacatttaactgggcattctgtatttaattggtaatctg agatggcagggaacagcatcagcatggtgtgagggataggca ttttttcattgtgtacagcttgtaaatcagtatttttaaaac tcaaagttaatggcttgggcatatttagaaaagagttgccgc acggacttgaaccctgtattcctaaaatctaggatcttgttc tgatggtctgcacaactggctgggggtgtccagccactgtcc ctcttgcctgggctccccagggcagttctgtcagcctctcca tttccattcctgttccagcaaaacccaactgatagcacagca gcatttcagcctgtctacctctgtgcccacatacctggatgt ctaccagccagaaaggtggcttagatttggttcctgtgggtg gattatggcccccagaacttccctgtgcttgctgggggtgtg gagtggaaagagcaggaaatgggggaccctccgatactctat gggggtcctccaagtctctttgtgcaagttagggtaataatc aatatggagctaagaaagagaaggggaactatgctttagaac aggacactgtgccaggagcattgcagaaattatatggttttc acgacagttctttttggtaggtactgttattatcctcagttt gcagatgaggaaactgagacccagaaaggttaaataacttgc tagggtcacacaagtcataactgacaaagcctgattcaaacc caggtctccctaacctttaaggtttctatgacgccagctctc ctagggagtttgtcttcagatgtcttggctctaggtgtcaaa aaaagacttggtgtcaggcaggcataggttcaagtcccaact ctgtcacttaccaactgtgactaggtgattgaactgaccatg gaacctggtcacatgcaggagcaggatggtgaagggttcttg aaggcacttaggcaggacatttaggcaggagagaaaacctgg aaacagaagagctgtctccaaaaatacccactggggaagcag gttgtcatgtgggccatgaatgggacctgttctggggtaacc acgtgcggaccgagcggccgcaggaacccctagtgatggagt tggccactccctctctgcgcgctcgctcgctcactgaggccg ggcgaccaaaggtcgcccgacgcccgggctttgcccgggcgg cctcagtgagcgagcgagcgcgcag Plasmid TM039 Composition 5′ ITR  2 occurs at bp 1 through bp 119 of SEQ ID NO: 29 CVM ENHANCER 22 AND CBA occurs at bp 134 through bp 1749 of SEQ ID PROMOTER NO: 29 GENBANK ACCESSION DD215332 FROM BP 1-BP 1616) Added Kozak  5 occurs at bp 1763 through bp 1768 of SEQ ID NO: 29 HUMAN RLBP1  6 GENE CDS occurs at bp 1769 through bp 2722 of SEQ ID NO: 29 SV40 POLYA  8 occurs at bp 2781 through bp 3016 of SEQ ID NO: 29 REVERSE 23 COMPLEMENT OF occurs at bp 3032 through bp 4534 of SEQ RLBP1 INTRONIC ID NO: 29 SEQUENCE AS STUFFER SEQUENCE (NT 010274.17) 3′ ITR  9 occurs at bp 4573 through bp 4702 of SEQ ID NO: 29 AMP BACTERIAL 15 BACKBONE occurs at bp 4703 through bp 7321 of SEQ ID NO: 29 PLASMID TM039 29 SEQUENCE ctgcgcgctcgctcgctcactgaggccgcccgggcgtcgggc gacctttggtcgcccggcctcagtgagcgagcgagcgcgcag agagggagtggccaactccatcactaggggttcctgcggccg cacgcgtactagttattaatagtaatcaattacggggtcatt agttcatagcccatatatggagttccgcgttacataacttac ggtaaatggcccgcctggctgaccgcccaacgacccccgccc attgacgtcaataatgacgtatgttcccatagtaacgccaat agggactttccattgacgtcaatgggtggagtatttacggta aactgcccacttggcagtacatcaagtgtatcatatgccaag tacgccccctattgacgtcaatgacggtaaatggcccgcctg gcattatgcccagtacatgaccttatgggactttcctacttg gcagtacatctacgtattagtcatcgctattaccatggtcga ggtgagccccacgttctgcttcactctccccatctccccccc ctccccacccccaattttgtatttatttattttttaattatt ttgtgcagcgatgggggcggggggggggggggggcgcgcgcc aggcggggcggggcggggcgaggggcggggcggggcgaggcg gagaggtgcggcggcagccaatcagagcggcgcgctccgaaa gtttccttttatggcgaggcggcggcggcggcggccctataa aaagcgaagcgcgcggcgggcggggagtcgctgcgacgctgc cttcgccccgtgccccgctccgccgccgcctcgcgccgcccg ccccggctctgactgaccgcgttactcccacaggtgagcggg cgggacggcccttctcctccgggctgtaattagcgcttggtt taatgacggcttgtttcttttctgtggctgcgtgaaagcctt gaggggctccgggagggccctttgtgcggggggagcggctcg gggggtgcgtgcgtgtgtgtgtgcgtggggagcgccgcgtgc ggctccgcgctgcccggcggctgtgagcgctgcgggcgcggc gcggggctttgtgcgctccgcagtgtgcgcgaggggagcgcg gccgggggcggtgccccgcggtgcggggggggctgcgagggg aacaaaggctgcgtgcggggtgtgtgcgtgggggggtgagca gggggtgtgggcgcgtcggtcgggctgcaaccccccctgcac ccccctccccgagttgctgagcacggcccggcttcgggtgcg gggctccgtacggggcgtggcgcggggctcgccgtgccgggc ggggggtggcggcaggtgggggtgccgggcggggcggggccg cctcgggccggggagggctcgggggaggggcgcggcggcccc cggagcgccggcggctgtcgaggcgcggcgagccgcagccat tgccttttatggtaatcgtgcgagagggcgcagggacttcct ttgtcccaaatctgtgcggagccgaaatctgggaggcgccgc cgcaccccctctagcgggcgcggggcgaagcggtgcggcgcc ggcaggaaggaaatgggcggggagggccttcgtgcgtcgccg cgccgccgtccccttctccctctccagcctcggggctgtccg cggggggacggctgccttcgggggggacggggcagggcgggg ttcggcttctggcgtgtgaccggcggcatcgattgaattcgc caccatgtcagaaggggtgggcacgttccgcatggtacctga agaggaacaggagctccgtgcccaactggagcagctcacaac caaggaccatggacctgtctttggcccgtgcagccagctgcc ccgccacaccttgcagaaggccaaggatgagctgaacgagag agaggagacccgggaggaggcagtgcgagagctgcaggagat ggtgcaggcgcaggcggcctcgggggaggagctggcggtggc cgtggcggagagggtgcaagagaaggacagcggcttcttcct gcgcttcatccgcgcacggaagttcaacgtgggccgtgccta tgagctgctcagaggctatgtgaatttccggctgcagtaccc tgagctctttgacagcctgtccccagaggctgtccgctgcac cattgaagctggctaccctggtgtcctctctagtcgggacaa gtatggccgagtggtcatgctcttcaacattgagaactggca aagtcaagaaatcacctttgatgagatcttgcaggcatattg cttcatcctggagaagctgctggagaatgaggaaactcaaat caatggcttctgcatcattgagaacttcaagggctttaccat gcagcaggctgctagtctccggacttcagatctcaggaagat ggtggacatgctccaggattccttcccagcccggttcaaagc catccacttcatccaccagccatggtacttcaccacgaccta caatgtggtcaagcccttcttgaagagcaagctgcttgagag ggtctttgtccacggggatgacctttctggtttctaccagga gatcgatgagaacatcctgccctctgacttcgggggcacgct gcccaagtatgatggcaaggccgttgctgagcagctctttgg cccccaggcccaagctgagaacacagccttctgaggatcgta ccggtcgacctgcagaagcttgcctcgagcagcgctgctcga gagatctggatcataatcagccataccacatttgtagaggtt ttacttgctttaaaaaacctcccacacctccccctgaacctg aaacataaaatgaatgcaattgttgttgttaacttgtttatt gcagcttataatggttacaaataaagcaatagcatcacaaat ttcacaaataaagcatttttttcactgcattctagttgtggt ttgtccaaactcatcaatgtatcttatcatgtctggtactag ggttaccccagaacaggtcccattcatggcccacatgacaac ctgcttccccagtgggtatttttggagacagctcttctgttt ccaggttttctctcctgcctaaatgtcctgcctaagtgcctt caagaacccttcaccatcctgctcctgcatgtgaccaggttc catggtcagttcaatcacctagtcacagttggtaagtgacag agttgggacttgaacctatgcctgcctgacaccaagtctttt tttgacacctagagccaagacatctgaagacaaactccctag gagagctggcgtcatagaaaccttaaaggttagggagacctg ggtttgaatcaggctttgtcagttatgacttgtgtgacccta gcaagttatttaacctttctgggtctcagtttcctcatctgc aaactgaggataataacagtacctaccaaaaagaactgtcgt gaaaaccatataatttctgcaatgctcctggcacagtgtcct gttctaaagcatagttccccttctctttcttagctccatatt gattattaccctaacttgcacaaagagacttggaggaccccc atagagtatcggagggtcccccatttcctgctctttccactc cacacccccagcaagcacagggaagttctgggggccataatc cacccacaggaaccaaatctaagccacctttctggctggtag acatccaggtatgtgggcacagaggtagacaggctgaaatgc tgctgtgctatcagttgggttttgctggaacaggaatggaaa tggagaggctgacagaactgccctggggagcccaggcaagag ggacagtggctggacacccccagccagttgtgcagaccatca gaacaagatcctagattttaggaatacagggttcaagtccgt gcggcaactcttttctaaatatgcccaagccattaactttga gttttaaaaatactgatttacaagctgtacacaatgaaaaaa tgcctatccctcacaccatgctgatgctgttccctgccatct cagattaccaattaaatacagaatgcccagttaaatgtgaac tttttttttttttttttttttgagatggagttttgttcttgt cgcccaggctagagtgcaatggtgcgatctcagctcactgca acctctgcctcccaggttcaagcaattctcctgccttagcct cctgagtagctggaactacaggtgcccaccagcacgcctggc taatttttggtatttttagtggagatggggtttcaccatgtt ggccaggctggtctcgaactcctgacctcaggtgatctgcct gcctcggcctcccaaagtgctgggattacaggcgtgagccta aatgtgaacttttttaatactaaaaaagtatttgctgttcat cggaaattcacatttaactgggtgtcctgtatttttatttgc taaatctaccatcaaattggtctggctcaacctggagaatgg ttaccctaggtaaccacgtgcggaccgagcggccgcaggaac ccctagtgatggagttggccactccctctctgcgcgctcgct cgctcactgaggccgggcgaccaaaggtcgcccgacgcccgg gctttgcccgggcggcctcagtgagcgagcgagcgcgcagct gcctgcaggggcgcctgatgcggtattttctccttacgcatc tgtgcggtatttcacaccgcatacgtcaaagcaaccatagta cgcgccctgtagcggcgcattaagcgcggcgggtgtggtggt tacgcgcagcgtgaccgctacacttgccagcgccttagcgcc cgctcctttcgctttcttcccttcctttctcgccacgttcgc cggctttccccgtcaagctctaaatcgggggctccctttagg gttccgatttagtgctttacggcacctcgaccccaaaaaact tgatttgggtgatggttcacgtagtgggccatcgccctgata gacggtttttcgccctttgacgttggagtccacgttctttaa tagtggactcttgttccaaactggaacaacactcaactctat ctcgggctattcttttgatttataagggattttgccgatttc ggtctattggttaaaaaatgagctgatttaacaaaaatttaa cgcgaattttaacaaaatattaacgtttacaattttatggtg cactctcagtacaatctgctctgatgccgcatagttaagcca gccccgacacccgccaacacccgctgacgcgccctgacgggc ttgtctgctcccggcatccgcttacagacaagctgtgaccgt ctccgggagctgcatgtgtcagaggttttcaccgtcatcacc gaaacgcgcgagacgaaagggcctcgtgatacgcctattttt ataggttaatgtcatgataataatggtttcttagacgtcagg tggcacttttcggggaaatgtgcgcggaacccctatttgttt atttttctaaatacattcaaatatgtatccgctcatgagaca ataaccctgataaatgcttcaataatattgaaaaaggaagag tatgagtattcaacatttccgtgtcgcccttattcccttttt tgcggcattttgccttcctgtttttgctcacccagaaacgct ggtgaaagtaaaagatgctgaagatcagttgggtgcacgagt gggttacatcgaactggatctcaacagcggtaagatccttga gagttttcgccccgaagaacgttttccaatgatgagcacttt taaagttctgctatgtggcgcggtattatcccgtattgacgc cgggcaagagcaactcggtcgccgcatacactattctcagaa tgacttggttgagtactcaccagtcacagaaaagcatcttac ggatggcatgacagtaagagaattatgcagtgctgccataac catgagtgataacactgcggccaacttacttctgacaacgat cggaggaccgaaggagctaaccgcttttttgcacaacatggg ggatcatgtaactcgccttgatcgttgggaaccggagctgaa tgaagccataccaaacgacgagcgtgacaccacgatgcctgt agcaatggcaacaacgttgcgcaaactattaactggcgaact acttactctagcttcccggcaacaattaatagactggatgga ggcggataaagttgcaggaccacttctgcgctcggcccttcc ggctggctggtttattgctgataaatctggagccggtgagcg tgggtctcgcggtatcattgcagcactggggccagatggtaa gccctcccgtatcgtagttatctacacgacggggagtcaggc aactatggatgaacgaaatagacagatcgctgagataggtgc ctcactgattaagcattggtaactgtcagaccaagtttactc atatatactttagattgatttaaaacttcatttttaatttaa aaggatctaggtgaagatcctttttgataatctcatgaccaa aatcccttaacgtgagttttcgttccactgagcgtcagaccc cgtagaaaagatcaaaggatcttcttgaaatcctttttttct gcgcgtaatctgctgcttgcaaacaaaaaaaccaccgctacc agcggtggtttgtttgccggatcaagagctaccaactctttt tccgaaggtaactggcttcagcagagcgcagataccaaatac tgttcttctagtgtagccgtagttaggccaccacttcaagaa ctctgtagcaccgcctacatacctcgctctgctaatcctgtt accagtggctgctgccagtggcgataagtcgtgtcttaccgg gttggactcaagacgatagttaccggataaggcgcagcggtc gggctgaacggggggttcgtgcacacagcccagcttggagcg aacgacctacaccgaactgagatacctacagcgtgagctatg agaaagcgccacgcttcccgaagggagaaaggcggacaggta tccggtaagcggcagggtcggaacaggagagcgcacgaggga gcttccagggggaaacgcctggtatctttatagtcctgtcgg gtttcgccacctctgacttgagcgtcgatttttgtgatgctc gtcaggggggcggagcctatggaaaaacgccagcaacgcggc ctttttacggttcctggccttttgctggccttttgctcacat gtcctgcaggcag GENE CASSETTE 54 OF PLASMID ctgcgcgctcgctcgctcactgaggccgcccgggcgtcgggc TM039 OCCURS AT gacctttggtcgcccggcctcagtgagcgagcgagcgcgcag BP 1 THROUGH agagggagtggccaactccatcactaggggttcctgcggccg 4702 OF SEQ ID cacgcgtactagttattaatagtaatcaattacggggtcatt NO: 29 agttcatagcccatatatggagttccgcgttacataacttac ggtaaatggcccgcctggctgaccgcccaacgacccccgccc attgacgtcaataatgacgtatgttcccatagtaacgccaat agggactttccattgacgtcaatgggtggagtatttacggta aactgcccacttggcagtacatcaagtgtatcatatgccaag tacgccccctattgacgtcaatgacggtaaatggcccgcctg gcattatgcccagtacatgaccttatgggactttcctacttg gcagtacatctacgtattagtcatcgctattaccatggtcga ggtgagccccacgttctgcttcactctccccatctccccccc ctccccacccccaattttgtatttatttattttttaattatt ttgtgcagcgatgggggcggggggggggggggggcgcgcgcc aggcggggcggggcggggcgaggggcggggcggggcgaggcg gagaggtgcggcggcagccaatcagagcggcgcgctccgaaa gtttccttttatggcgaggcggcggcggcggcggccctataa aaagcgaagcgcgcggcgggcggggagtcgctgcgacgctgc cttcgccccgtgccccgctccgccgccgcctcgcgccgcccg ccccggctctgactgaccgcgttactcccacaggtgagcggg cgggacggcccttctcctccgggctgtaattagcgcttggtt taatgacggcttgtttcttttctgtggctgcgtgaaagcctt gaggggctccgggagggccctttgtgcggggggagcggctcg gggggtgcgtgcgtgtgtgtgtgcgtggggagcgccgcgtgc ggctccgcgctgcccggcggctgtgagcgctgcgggcgcggc gcggggctttgtgcgctccgcagtgtgcgcgaggggagcgcg gccgggggcggtgccccgcggtgcggggggggctgcgagggg aacaaaggctgcgtgcggggtgtgtgcgtgggggggtgagca gggggtgtgggcgcgtcggtcgggctgcaaccccccctgcac ccccctccccgagttgctgagcacggcccggcttcgggtgcg gggctccgtacggggcgtggcgcggggctcgccgtgccgggc ggggggtggcggcaggtgggggtgccgggcggggcggggccg cctcgggccggggagggctcgggggaggggcgcggcggcccc cggagcgccggcggctgtcgaggcgcggcgagccgcagccat tgccttttatggtaatcgtgcgagagggcgcagggacttcct ttgtcccaaatctgtgcggagccgaaatctgggaggcgccgc cgcaccccctctagcgggcgcggggcgaagcggtgcggcgcc ggcaggaaggaaatgggcggggagggccttcgtgcgtcgccg cgccgccgtccccttctccctctccagcctcggggctgtccg cggggggacggctgccttcgggggggacggggcagggcgggg ttcggcttctggcgtgtgaccggcggcatcgattgaattcgc caccatgtcagaaggggtgggcacgttccgcatggtacctga agaggaacaggagctccgtgcccaactggagcagctcacaac caaggaccatggacctgtctttggcccgtgcagccagctgcc ccgccacaccttgcagaaggccaaggatgagctgaacgagag agaggagacccgggaggaggcagtgcgagagctgcaggagat ggtgcaggcgcaggcggcctcgggggaggagctggcggtggc cgtggcggagagggtgcaagagaaggacagcggcttcttcct gcgcttcatccgcgcacggaagttcaacgtgggccgtgccta tgagctgctcagaggctatgtgaatttccggctgcagtaccc tgagctctttgacagcctgtccccagaggctgtccgctgcac cattgaagctggctaccctggtgtcctctctagtcgggacaa gtatggccgagtggtcatgctcttcaacattgagaactggca aagtcaagaaatcacctttgatgagatcttgcaggcatattg cttcatcctggagaagctgctggagaatgaggaaactcaaat caatggcttctgcatcattgagaacttcaagggctttaccat gcagcaggctgctagtctccggacttcagatctcaggaagat ggtggacatgctccaggattccttcccagcccggttcaaagc catccacttcatccaccagccatggtacttcaccacgaccta caatgtggtcaagcccttcttgaagagcaagctgcttgagag ggtctttgtccacggggatgacctttctggtttctaccagga gatcgatgagaacatcctgccctctgacttcgggggcacgct gcccaagtatgatggcaaggccgttgctgagcagctctttgg cccccaggcccaagctgagaacacagccttctgaggatcgta ccggtcgacctgcagaagcttgcctcgagcagcgctgctcga gagatctggatcataatcagccataccacatttgtagaggtt ttacttgctttaaaaaacctcccacacctccccctgaacctg aaacataaaatgaatgcaattgttgttgttaacttgtttatt gcagcttataatggttacaaataaagcaatagcatcacaaat ttcacaaataaagcatttttttcactgcattctagttgtggt ttgtccaaactcatcaatgtatcttatcatgtctggtactag ggttaccccagaacaggtcccattcatggcccacatgacaac ctgcttccccagtgggtatttttggagacagctcttctgttt ccaggttttctctcctgcctaaatgtcctgcctaagtgcctt caagaacccttcaccatcctgctcctgcatgtgaccaggttc catggtcagttcaatcacctagtcacagttggtaagtgacag agttgggacttgaacctatgcctgcctgacaccaagtctttt tttgacacctagagccaagacatctgaagacaaactccctag gagagctggcgtcatagaaaccttaaaggttagggagacctg ggtttgaatcaggctttgtcagttatgacttgtgtgacccta gcaagttatttaacctttctgggtctcagtttcctcatctgc aaactgaggataataacagtacctaccaaaaagaactgtcgt gaaaaccatataatttctgcaatgctcctggcacagtgtcct gttctaaagcatagttccccttctctttcttagctccatatt gattattaccctaacttgcacaaagagacttggaggaccccc atagagtatcggagggtcccccatttcctgctctttccactc cacacccccagcaagcacagggaagttctgggggccataatc cacccacaggaaccaaatctaagccacctttctggctggtag acatccaggtatgtgggcacagaggtagacaggctgaaatgc tgctgtgctatcagttgggttttgctggaacaggaatggaaa tggagaggctgacagaactgccctggggagcccaggcaagag ggacagtggctggacacccccagccagttgtgcagaccatca gaacaagatcctagattttaggaatacagggttcaagtccgt gcggcaactcttttctaaatatgcccaagccattaactttga gttttaaaaatactgatttacaagctgtacacaatgaaaaaa tgcctatccctcacaccatgctgatgctgttccctgccatct cagattaccaattaaatacagaatgcccagttaaatgtgaac tttttttttttttttttttttgagatggagttttgttcttgt cgcccaggctagagtgcaatggtgcgatctcagctcactgca acctctgcctcccaggttcaagcaattctcctgccttagcct cctgagtagctggaactacaggtgcccaccagcacgcctggc taatttttggtatttttagtggagatggggtttcaccatgtt ggccaggctggtctcgaactcctgacctcaggtgatctgcct gcctcggcctcccaaagtgctgggattacaggcgtgagccta aatgtgaacttttttaatactaaaaaagtatttgctgttcat cggaaattcacatttaactgggtgtcctgtatttttatttgc taaatctaccatcaaattggtctggctcaacctggagaatgg ttaccctaggtaaccacgtgcggaccgagcggccgcaggaac ccctagtgatggagttggccactccctctctgcgcgctcgct cgctcactgaggccgggcgaccaaaggtcgcccgacgcccgg gctttgcccgggcggcctcagtgagcgagcgagcgcgcag Plasmid TM040 Composition 5′ ITR  2 occurs at bp 1 through bp 119 of SEQ ID NO: 30 Human RLBP1  3 Promoter(short) occurs at bp 134 through bp 723 of SEQ ID NO: 30 Modified SV40  4 intron occurs at bp 738 through bp 920 of SEQ ID NO: 30 Added Kozak  5 occurs at bp 934 through bp 939 of SEQ ID NO: 30 HUMAN RLBP1  6 GENE CDS occurs at bp 940 through bp 1893 of SEQ ID NO: 30 SV40 POLYA  8 occurs at bp 1952 through bp 2187 of SEQ ID NO: 30 REVERSE 23 COMPLEMENT OF occurs at bp 2203 through bp 3705 of SEQ RLBP1 INTRONIC ID NO: 30 SEQUENCE AS STUFFER SEQUENCE (NT 010274.17) 3′ ITR  9 occurs at bp 3744 through bp 3873 of SEQ ID NO: 30 AMP BACTERIAL 15 BACKBONE occurs at bp 3874 through bp 6492 of SEQ ID NO: 30 TM040 plasmid 30 sequence ctgcgcgctcgctcgctcactgaggccgcccgggcgtcgggc gacctttggtcgcccggcctcagtgagcgagcgagcgcgcag agagggagtggccaactccatcactaggggttcctgcggccg cacgcgtttgtcctctccctgcttggccttaaccagccacat ttctcaactgaccccactcactgcagaggtgaaaactaccat gccaggtcctgctggctgggggaggggtgggcaataggcctg gatttgccagagctgccactgtagatgtagtcatatttacga tttcccttcacctcttattaccctggtggtggtggtgggggg gggggggtgctctctcagcaaccccaccccgggatcttgagg agaaagagggcagagaaaagagggaatgggactggcccagat cccagccccacagccgggcttccacatggccgagcaggaact ccagagcaggagcacacaaaggagggctttgatgcgcctcca gccaggcccaggcctctcccctctcccctttctctctgggtc ttcctttgccccactgagggcctcctgtgagcccgatttaac ggaaactgtgggcggtgagaagttccttatgacacactaatc ccaacctgctgaccggaccacgcctccagcggagggaacctc tagagctccaggacattcaggtaccaggtagccccaaggagg agctgccgaatcgatggatcgggaactgaaaaaccagaaagt taactggtaagtttagtctttttgtcttttatttcaggtccc ggatccggtggtggtgcaaatcaaagaactgctcctcagtgg atgttgcctttacttctaggcctgtacggaagtgttacttct gctctaaaagctgcggaattgtacccgccccgggatccatcg attgaattcgccaccatgtcagaaggggtgggcacgttccgc atggtacctgaagaggaacaggagctccgtgcccaactggag cagctcacaaccaaggaccatggacctgtctttggcccgtgc agccagctgccccgccacaccttgcagaaggccaaggatgag ctgaacgagagagaggagacccgggaggaggcagtgcgagag ctgcaggagatggtgcaggcgcaggcggcctcgggggaggag ctggcggtggccgtggcggagagggtgcaagagaaggacagc ggcttcttcctgcgcttcatccgcgcacggaagttcaacgtg ggccgtgcctatgagctgctcagaggctatgtgaatttccgg ctgcagtaccctgagctctttgacagcctgtccccagaggct gtccgctgcaccattgaagctggctaccctggtgtcctctct agtcgggacaagtatggccgagtggtcatgctcttcaacatt gagaactggcaaagtcaagaaatcacctttgatgagatcttg caggcatattgcttcatcctggagaagctgctggagaatgag gaaactcaaatcaatggcttctgcatcattgagaacttcaag ggctttaccatgcagcaggctgctagtctccggacttcagat ctcaggaagatggtggacatgctccaggattccttcccagcc cggttcaaagccatccacttcatccaccagccatggtacttc accacgacctacaatgtggtcaagcccttcttgaagagcaag ctgcttgagagggtctttgtccacggggatgacctttctggt ttctaccaggagatcgatgagaacatcctgccctctgacttc gggggcacgctgcccaagtatgatggcaaggccgttgctgag cagctctttggcccccaggcccaagctgagaacacagccttc tgaggatcgtaccggtcgacctgcagaagcttgcctcgagca gcgctgctcgagagatctggatcataatcagccataccacat ttgtagaggttttacttgctttaaaaaacctcccacacctcc ccctgaacctgaaacataaaatgaatgcaattgttgttgtta acttgtttattgcagcttataatggttacaaataaagcaata gcatcacaaatttcacaaataaagcatttttttcactgcatt ctagttgtggtttgtccaaactcatcaatgtatcttatcatg tctggtactagggttaccccagaacaggtcccattcatggcc cacatgacaacctgcttccccagtgggtatttttggagacag ctcttctgtttccaggttttctctcctgcctaaatgtcctgc ctaagtgccttcaagaacccttcaccatcctgctcctgcatg tgaccaggttccatggtcagttcaatcacctagtcacagttg gtaagtgacagagttgggacttgaacctatgcctgcctgaca ccaagtctttttttgacacctagagccaagacatctgaagac aaactccctaggagagctggcgtcatagaaaccttaaaggtt agggagacctgggtttgaatcaggctttgtcagttatgactt gtgtgaccctagcaagttatttaacctttctgggtctcagtt tcctcatctgcaaactgaggataataacagtacctaccaaaa agaactgtcgtgaaaaccatataatttctgcaatgctcctgg cacagtgtcctgttctaaagcatagttccccttctctttctt agctccatattgattattaccctaacttgcacaaagagactt ggaggacccccatagagtatcggagggtcccccatttcctgc tctttccactccacacccccagcaagcacagggaagttctgg gggccataatccacccacaggaaccaaatctaagccaccttt ctggctggtagacatccaggtatgtgggcacagaggtagaca ggctgaaatgctgctgtgctatcagttgggttttgctggaac aggaatggaaatggagaggctgacagaactgccctggggagc ccaggcaagagggacagtggctggacacccccagccagttgt gcagaccatcagaacaagatcctagattttaggaatacaggg ttcaagtccgtgcggcaactcttttctaaatatgcccaagcc attaactttgagttttaaaaatactgatttacaagctgtaca caatgaaaaaatgcctatccctcacaccatgctgatgctgtt ccctgccatctcagattaccaattaaatacagaatgcccagt taaatgtgaactttttttttttttttttttttgagatggagt tttgttcttgtcgcccaggctagagtgcaatggtgcgatctc agctcactgcaacctctgcctcccaggttcaagcaattctcc tgccttagcctcctgagtagctggaactacaggtgcccacca gcacgcctggctaatttttggtatttttagtggagatggggt ttcaccatgttggccaggctggtctcgaactcctgacctcag gtgatctgcctgcctcggcctcccaaagtgctgggattacag gcgtgagcctaaatgtgaacttttttaatactaaaaaagtat ttgctgttcatcggaaattcacatttaactgggtgtcctgta tttttatttgctaaatctaccatcaaattggtctggctcaac ctggagaatggttaccctaggtaaccacgtgcggaccgagcg gccgcaggaacccctagtgatggagttggccactccctctct gcgcgctcgctcgctcactgaggccgggcgaccaaaggtcgc ccgacgcccgggctttgcccgggcggcctcagtgagcgagcg agcgcgcagctgcctgcaggggcgcctgatgcggtattttct ccttacgcatctgtgcggtatttcacaccgcatacgtcaaag caaccatagtacgcgccctgtagcggcgcattaagcgcggcg ggtgtggtggttacgcgcagcgtgaccgctacacttgccagc gccttagcgcccgctcctttcgctttcttcccttcctttctc gccacgttcgccggctttccccgtcaagctctaaatcggggg ctccctttagggttccgatttagtgctttacggcacctcgac cccaaaaaacttgatttgggtgatggttcacgtagtgggcca tcgccctgatagacggtttttcgccctttgacgttggagtcc acgttctttaatagtggactcttgttccaaactggaacaaca ctcaactctatctcgggctattcttttgatttataagggatt ttgccgatttcggtctattggttaaaaaatgagctgatttaa caaaaatttaacgcgaattttaacaaaatattaacgtttaca attttatggtgcactctcagtacaatctgctctgatgccgca tagttaagccagccccgacacccgccaacacccgctgacgcg ccctgacgggcttgtctgctcccggcatccgcttacagacaa gctgtgaccgtctccgggagctgcatgtgtcagaggttttca ccgtcatcaccgaaacgcgcgagacgaaagggcctcgtgata cgcctatttttataggttaatgtcatgataataatggtttct tagacgtcaggtggcacttttcggggaaatgtgcgcggaacc cctatttgtttatttttctaaatacattcaaatatgtatccg ctcatgagacaataaccctgataaatgcttcaataatattga aaaaggaagagtatgagtattcaacatttccgtgtcgccctt attcccttttttgcggcattttgccttcctgtttttgctcac ccagaaacgctggtgaaagtaaaagatgctgaagatcagttg ggtgcacgagtgggttacatcgaactggatctcaacagcggt aagatccttgagagttttcgccccgaagaacgttttccaatg atgagcacttttaaagttctgctatgtggcgcggtattatcc cgtattgacgccgggcaagagcaactcggtcgccgcatacac tattctcagaatgacttggttgagtactcaccagtcacagaa aagcatcttacggatggcatgacagtaagagaattatgcagt gctgccataaccatgagtgataacactgcggccaacttactt ctgacaacgatcggaggaccgaaggagctaaccgcttttttg cacaacatgggggatcatgtaactcgccttgatcgttgggaa ccggagctgaatgaagccataccaaacgacgagcgtgacacc acgatgcctgtagcaatggcaacaacgttgcgcaaactatta actggcgaactacttactctagcttcccggcaacaattaata gactggatggaggcggataaagttgcaggaccacttctgcgc tcggcccttccggctggctggtttattgctgataaatctgga gccggtgagcgtgggtctcgcggtatcattgcagcactgggg ccagatggtaagccctcccgtatcgtagttatctacacgacg gggagtcaggcaactatggatgaacgaaatagacagatcgct gagataggtgcctcactgattaagcattggtaactgtcagac caagtttactcatatatactttagattgatttaaaacttcat ttttaatttaaaaggatctaggtgaagatcctttttgataat ctcatgaccaaaatcccttaacgtgagttttcgttccactga gcgtcagaccccgtagaaaagatcaaaggatcttcttgaaat cctttttttctgcgcgtaatctgctgcttgcaaacaaaaaaa ccaccgctaccagcggtggtttgtttgccggatcaagagcta ccaactctttttccgaaggtaactggcttcagcagagcgcag ataccaaatactgttcttctagtgtagccgtagttaggccac cacttcaagaactctgtagcaccgcctacatacctcgctctg ctaatcctgttaccagtggctgctgccagtggcgataagtcg tgtcttaccgggttggactcaagacgatagttaccggataag gcgcagcggtcgggctgaacggggggttcgtgcacacagccc agcttggagcgaacgacctacaccgaactgagatacctacag cgtgagctatgagaaagcgccacgcttcccgaagggagaaag gcggacaggtatccggtaagcggcagggtcggaacaggagag cgcacgagggagcttccagggggaaacgcctggtatctttat agtcctgtcgggtttcgccacctctgacttgagcgtcgattt ttgtgatgctcgtcaggggggcggagcctatggaaaaacgcc agcaacgcggcctttttacggttcctggccttttgctggcct tttgctcacatgtcctgcaggcag GENE CASSETTE 55 OF PLASMID ctgcgcgctcgctcgctcactgaggccgcccgggcgtcgggc TM040 OCCURS AT gacctttggtcgcccggcctcagtgagcgagcgagcgcgcag BP 1 THROUGH agagggagtggccaactccatcactaggggttcctgcggccg 3873 OF SEQ ID cacgcgtttgtcctctccctgcttggccttaaccagccacat NO: 30 ttctcaactgaccccactcactgcagaggtgaaaactaccat gccaggtcctgctggctgggggaggggtgggcaataggcctg gatttgccagagctgccactgtagatgtagtcatatttacga tttcccttcacctcttattaccctggtggtggtggtgggggg gggggggtgctctctcagcaaccccaccccgggatcttgagg agaaagagggcagagaaaagagggaatgggactggcccagat cccagccccacagccgggcttccacatggccgagcaggaact ccagagcaggagcacacaaaggagggctttgatgcgcctcca gccaggcccaggcctctcccctctcccctttctctctgggtc ttcctttgccccactgagggcctcctgtgagcccgatttaac ggaaactgtgggcggtgagaagttccttatgacacactaatc ccaacctgctgaccggaccacgcctccagcggagggaacctc tagagctccaggacattcaggtaccaggtagccccaaggagg agctgccgaatcgatggatcgggaactgaaaaaccagaaagt taactggtaagtttagtctttttgtcttttatttcaggtccc ggatccggtggtggtgcaaatcaaagaactgctcctcagtgg atgttgcctttacttctaggcctgtacggaagtgttacttct gctctaaaagctgcggaattgtacccgccccgggatccatcg attgaattcgccaccatgtcagaaggggtgggcacgttccgc atggtacctgaagaggaacaggagctccgtgcccaactggag cagctcacaaccaaggaccatggacctgtctttggcccgtgc agccagctgccccgccacaccttgcagaaggccaaggatgag ctgaacgagagagaggagacccgggaggaggcagtgcgagag ctgcaggagatggtgcaggcgcaggcggcctcgggggaggag ctggcggtggccgtggcggagagggtgcaagagaaggacagc ggcttcttcctgcgcttcatccgcgcacggaagttcaacgtg ggccgtgcctatgagctgctcagaggctatgtgaatttccgg ctgcagtaccctgagctctttgacagcctgtccccagaggct gtccgctgcaccattgaagctggctaccctggtgtcctctct agtcgggacaagtatggccgagtggtcatgctcttcaacatt gagaactggcaaagtcaagaaatcacctttgatgagatcttg caggcatattgcttcatcctggagaagctgctggagaatgag gaaactcaaatcaatggcttctgcatcattgagaacttcaag ggctttaccatgcagcaggctgctagtctccggacttcagat ctcaggaagatggtggacatgctccaggattccttcccagcc cggttcaaagccatccacttcatccaccagccatggtacttc accacgacctacaatgtggtcaagcccttcttgaagagcaag ctgcttgagagggtctttgtccacggggatgacctttctggt ttctaccaggagatcgatgagaacatcctgccctctgacttc gggggcacgctgcccaagtatgatggcaaggccgttgctgag cagctctttggcccccaggcccaagctgagaacacagccttc tgaggatcgtaccggtcgacctgcagaagcttgcctcgagca gcgctgctcgagagatctggatcataatcagccataccacat ttgtagaggttttacttgctttaaaaaacctcccacacctcc ccctgaacctgaaacataaaatgaatgcaattgttgttgtta acttgtttattgcagcttataatggttacaaataaagcaata gcatcacaaatttcacaaataaagcatttttttcactgcatt ctagttgtggtttgtccaaactcatcaatgtatcttatcatg tctggtactagggttaccccagaacaggtcccattcatggcc cacatgacaacctgcttccccagtgggtatttttggagacag ctcttctgtttccaggttttctctcctgcctaaatgtcctgc ctaagtgccttcaagaacccttcaccatcctgctcctgcatg tgaccaggttccatggtcagttcaatcacctagtcacagttg gtaagtgacagagttgggacttgaacctatgcctgcctgaca ccaagtctttttttgacacctagagccaagacatctgaagac aaactccctaggagagctggcgtcatagaaaccttaaaggtt agggagacctgggtttgaatcaggctttgtcagttatgactt gtgtgaccctagcaagttatttaacctttctgggtctcagtt tcctcatctgcaaactgaggataataacagtacctaccaaaa agaactgtcgtgaaaaccatataatttctgcaatgctcctgg cacagtgtcctgttctaaagcatagttccccttctctttctt agctccatattgattattaccctaacttgcacaaagagactt ggaggacccccatagagtatcggagggtcccccatttcctgc tctttccactccacacccccagcaagcacagggaagttctgg gggccataatccacccacaggaaccaaatctaagccaccttt ctggctggtagacatccaggtatgtgggcacagaggtagaca ggctgaaatgctgctgtgctatcagttgggttttgctggaac aggaatggaaatggagaggctgacagaactgccctggggagc ccaggcaagagggacagtggctggacacccccagccagttgt gcagaccatcagaacaagatcctagattttaggaatacaggg ttcaagtccgtgcggcaactcttttctaaatatgcccaagcc attaactttgagttttaaaaatactgatttacaagctgtaca caatgaaaaaatgcctatccctcacaccatgctgatgctgtt ccctgccatctcagattaccaattaaatacagaatgcccagt taaatgtgaactttttttttttttttttttttgagatggagt tttgttcttgtcgcccaggctagagtgcaatggtgcgatctc agctcactgcaacctctgcctcccaggttcaagcaattctcc tgccttagcctcctgagtagctggaactacaggtgcccacca gcacgcctggctaatttttggtatttttagtggagatggggt ttcaccatgttggccaggctggtctcgaactcctgacctcag gtgatctgcctgcctcggcctcccaaagtgctgggattacag gcgtgagcctaaatgtgaacttttttaatactaaaaaagtat ttgctgttcatcggaaattcacatttaactgggtgtcctgta tttttatttgctaaatctaccatcaaattggtctggctcaac ctggagaatggttaccctaggtaaccacgtgcggaccgagcg gccgcaggaacccctagtgatggagttggccactccctctct gcgcgctcgctcgctcactgaggccgggcgaccaaaggtcgc ccgacgcccgggctttgcccgggcggcctcagtgagcgagcg agcgcgcag Plasmid TM016 Composition Δ5′ ITR  1 occurs at bp 1 through bp 103 of SEQ ID NO: 31 Human RLBP1  3 Promoter(short) occurs at bp 116 through bp 705 of SEQ ID NO: 31 Modified SV40  4 intron occurs at bp 720 through bp 902 of SEQ ID NO: 31 Added Kozak  5 occurs at bp 943 through bp 948 of SEQ ID NO: 31 E_GFP 24 occurs at bp 949 through bp 1668 of SEQ ID NO: 31 SV40 POLYA  8 occurs at bp 1726 through bp 1961 of SEQ ID NO: 31 3′ ITR  9 occurs at bp 1990 through bp 2119 of SEQ ID NO: 31 AMP BACTERIAL 15 BACKBONE occurs at bp 2120 through bp 4738 of SEQ ID NO: 31 Sequence of 31 TM016 Plasmid cgcgctcgctcgctcactgaggccgcccgggcaaagcccggg cgtcgggcgacctttggtcgcccggcctcagtgagcgagcga gcgcgcagagagggagtggggtaccacgcgtttgtcctctcc ctgcttggccttaaccagccacatttctcaactgaccccact cactgcagaggtgaaaactaccatgccaggtcctgctggctg ggggaggggtgggcaataggcctggatttgccagagctgcca ctgtagatgtagtcatatttacgatttcccttcacctcttat taccctggtggtggtggtgggggggggggggtgctctctcag caaccccaccccgggatcttgaggagaaagagggcagagaaa agagggaatgggactggcccagatcccagccccacagccggg cttccacatggccgagcaggaactccagagcaggagcacaca aaggagggctttgatgcgcctccagccaggcccaggcctctc ccctctcccctttctctctgggtcttcctttgccccactgag ggcctcctgtgagcccgatttaacggaaactgtgggcggtga gaagttccttatgacacactaatcccaacctgctgaccggac cacgcctccagcggagggaacctctagagctccaggacattc aggtaccaggtagccccaaggaggagctgccgaatcgatgga tcgggaactgaaaaaccagaaagttaactggtaagtttagtc tttttgtcttttatttcaggtcccggatccggtggtggtgca aatcaaagaactgctcctcagtggatgttgcctttacttcta ggcctgtacggaagtgttacttctgctctaaaagctgcggaa ttgtacccgccccgggatccatcgattgaattccccggggat cctctagagtcgaaattcgccaccatggtgagcaagggcgag gagctgttcaccggggtggtgcccatcctggtcgagctggac ggcgacgtaaacggccacaagttcagcgtgtccggcgagggc gagggcgatgccacctacggcaagctgaccctgaagttcatc tgcaccaccggcaagctgcccgtgccctggcccaccctcgtg accaccctgacctacggcgtgcagtgcttcagccgctacccc gaccacatgaagcagcacgacttcttcaagtccgccatgccc gaaggctacgtccaggagcgcaccatcttcttcaaggacgac ggcaactacaagacccgcgccgaggtgaagttcgagggcgac accctggtgaaccgcatcgagctgaagggcatcgacttcaag gaggacggcaacatcctggggcacaagctggagtacaactac aacagccacaacgtctatatcatggccgacaagcagaagaac ggcatcaaggtgaacttcaagatccgccacaacatcgaggac ggcagcgtgcagctcgccgaccactaccagcagaacaccccc atcggcgacggccccgtgctgctgcccgacaaccactacctg agcacccagtccgccctgagcaaagaccccaacgagaagcgc gatcacatggtcctgctggagttcgtgaccgccgccgggatc actctcggcatggacgagctgtacaagtaatagggtaccggt cgacctgcagaagcttgcctcgagcagcgctgctcgagagat ctggatcataatcagccataccacatttgtagaggttttact tgctttaaaaaacctcccacacctccccctgaacctgaaaca taaaatgaatgcaattgttgttgttaacttgtttattgcagc ttataatggttacaaataaagcaatagcatcacaaatttcac aaataaagcatttttttcactgcattctagttgtggtttgtc caaactcatcaatgtatcttatcatgtctggtaaccacgtgc ggaccgagcggccgcaggaacccctagtgatggagttggcca ctccctctctgcgcgctcgctcgctcactgaggccgggcgac caaaggtcgcccgacgcccgggctttgcccgggcggcctcag tgagcgagcgagcgcgcagctgcctgcaggggcgcctgatgc ggtattttctccttacgcatctgtgcggtatttcacaccgca tacgtcaaagcaaccatagtacgcgccctgtagcggcgcatt aagcgcggcgggtgtggtggttacgcgcagcgtgaccgctac acttgccagcgccttagcgcccgctcctttcgctttcttccc ttcctttctcgccacgttcgccggctttccccgtcaagctct aaatcgggggctccctttagggttccgatttagtgctttacg gcacctcgaccccaaaaaacttgatttgggtgatggttcacg tagtgggccatcgccctgatagacggtttttcgccctttgac gttggagtccacgttctttaatagtggactcttgttccaaac tggaacaacactcaactctatctcgggctattcttttgattt ataagggattttgccgatttcggtctattggttaaaaaatga gctgatttaacaaaaatttaacgcgaattttaacaaaatatt aacgtttacaattttatggtgcactctcagtacaatctgctc tgatgccgcatagttaagccagccccgacacccgccaacacc cgctgacgcgccctgacgggcttgtctgctcccggcatccgc ttacagacaagctgtgaccgtctccgggagctgcatgtgtca gaggttttcaccgtcatcaccgaaacgcgcgagacgaaaggg cctcgtgatacgcctatttttataggttaatgtcatgataat aatggtttcttagacgtcaggtggcacttttcggggaaatgt gcgcggaacccctatttgtttatttttctaaatacattcaaa tatgtatccgctcatgagacaataaccctgataaatgcttca ataatattgaaaaaggaagagtatgagtattcaacatttccg tgtcgcccttattcccttttttgcggcattttgccttcctgt ttttgctcacccagaaacgctggtgaaagtaaaagatgctga agatcagttgggtgcacgagtgggttacatcgaactggatct caacagcggtaagatccttgagagttttcgccccgaagaacg ttttccaatgatgagcacttttaaagttctgctatgtggcgc ggtattatcccgtattgacgccgggcaagagcaactcggtcg ccgcatacactattctcagaatgacttggttgagtactcacc agtcacagaaaagcatcttacggatggcatgacagtaagaga attatgcagtgctgccataaccatgagtgataacactgcggc caacttacttctgacaacgatcggaggaccgaaggagctaac cgcttttttgcacaacatgggggatcatgtaactcgccttga tcgttgggaaccggagctgaatgaagccataccaaacgacga gcgtgacaccacgatgcctgtagcaatggcaacaacgttgcg caaactattaactggcgaactacttactctagcttcccggca acaattaatagactggatggaggcggataaagttgcaggacc acttctgcgctcggcccttccggctggctggtttattgctga taaatctggagccggtgagcgtgggtctcgcggtatcattgc agcactggggccagatggtaagccctcccgtatcgtagttat ctacacgacggggagtcaggcaactatggatgaacgaaatag acagatcgctgagataggtgcctcactgattaagcattggta actgtcagaccaagtttactcatatatactttagattgattt aaaacttcatttttaatttaaaaggatctaggtgaagatcct ttttgataatctcatgaccaaaatcccttaacgtgagttttc gttccactgagcgtcagaccccgtagaaaagatcaaaggatc ttcttgaaatcctttttttctgcgcgtaatctgctgcttgca aacaaaaaaaccaccgctaccagcggtggtttgtttgccgga tcaagagctaccaactctttttccgaaggtaactggcttcag cagagcgcagataccaaatactgttcttctagtgtagccgta gttaggccaccacttcaagaactctgtagcaccgcctacata cctcgctctgctaatcctgttaccagtggctgctgccagtgg cgataagtcgtgtcttaccgggttggactcaagacgatagtt accggataaggcgcagcggtcgggctgaacggggggttcgtg cacacagcccagcttggagcgaacgacctacaccgaactgag atacctacagcgtgagctatgagaaagcgccacgcttcccga agggagaaaggcggacaggtatccggtaagcggcagggtcgg aacaggagagcgcacgagggagcttccagggggaaacgcctg gtatctttatagtcctgtcgggtttcgccacctctgacttga gcgtcgatttttgtgatgctcgtcaggggggcggagcctatg gaaaaacgccagcaacgcggcctttttacggttcctggcctt ttgctggccttttgctcacatgtcctgcaggcagctg GENE CASSETTE 56 OF PLASMID cgcgctcgctcgctcactgaggccgcccgggcaaagcccggg TM016 OCCURS AT cgtcgggcgacctttggtcgcccggcctcagtgagcgagcga BP 1 THROUGH gcgcgcagagagggagtggggtaccacgcgtttgtcctctcc 2119 OF SEQ ID ctgcttggccttaaccagccacatttctcaactgaccccact NO: 31 cactgcagaggtgaaaactaccatgccaggtcctgctggctg ggggaggggtgggcaataggcctggatttgccagagctgcca ctgtagatgtagtcatatttacgatttcccttcacctcttat taccctggtggtggtggtgggggggggggggtgctctctcag caaccccaccccgggatcttgaggagaaagagggcagagaaa agagggaatgggactggcccagatcccagccccacagccggg cttccacatggccgagcaggaactccagagcaggagcacaca aaggagggctttgatgcgcctccagccaggcccaggcctctc ccctctcccctttctctctgggtcttcctttgccccactgag ggcctcctgtgagcccgatttaacggaaactgtgggcggtga gaagttccttatgacacactaatcccaacctgctgaccggac cacgcctccagcggagggaacctctagagctccaggacattc aggtaccaggtagccccaaggaggagctgccgaatcgatgga tcgggaactgaaaaaccagaaagttaactggtaagtttagtc tttttgtcttttatttcaggtcccggatccggtggtggtgca aatcaaagaactgctcctcagtggatgttgcctttacttcta ggcctgtacggaagtgttacttctgctctaaaagctgcggaa ttgtacccgccccgggatccatcgattgaattccccggggat cctctagagtcgaaattcgccaccatggtgagcaagggcgag gagctgttcaccggggtggtgcccatcctggtcgagctggac ggcgacgtaaacggccacaagttcagcgtgtccggcgagggc gagggcgatgccacctacggcaagctgaccctgaagttcatc tgcaccaccggcaagctgcccgtgccctggcccaccctcgtg accaccctgacctacggcgtgcagtgcttcagccgctacccc gaccacatgaagcagcacgacttcttcaagtccgccatgccc gaaggctacgtccaggagcgcaccatcttcttcaaggacgac ggcaactacaagacccgcgccgaggtgaagttcgagggcgac accctggtgaaccgcatcgagctgaagggcatcgacttcaag gaggacggcaacatcctggggcacaagctggagtacaactac aacagccacaacgtctatatcatggccgacaagcagaagaac ggcatcaaggtgaacttcaagatccgccacaacatcgaggac ggcagcgtgcagctcgccgaccactaccagcagaacaccccc atcggcgacggccccgtgctgctgcccgacaaccactacctg agcacccagtccgccctgagcaaagaccccaacgagaagcgc gatcacatggtcctgctggagttcgtgaccgccgccgggatc actctcggcatggacgagctgtacaagtaatagggtaccggt cgacctgcagaagcttgcctcgagcagcgctgctcgagagat ctggatcataatcagccataccacatttgtagaggttttact tgctttaaaaaacctcccacacctccccctgaacctgaaaca taaaatgaatgcaattgttgttgttaacttgtttattgcagc ttataatggttacaaataaagcaatagcatcacaaatttcac aaataaagcatttttttcactgcattctagttgtggtttgtc caaactcatcaatgtatcttatcatgtctggtaaccacgtgc ggaccgagcggccgcaggaacccctagtgatggagttggcca ctccctctctgcgcgctcgctcgctcactgaggccgggcgac caaaggtcgcccgacgcccgggctttgcccgggcggcctcag tgagcgagcgagcgcgcag Plasmid TM035 Composition 5′ ITR  2 occurs at bp 1 through bp 119 of SEQ ID NO: 32 Human RLBP1 10 Promoter(long) occurs at bp 137 through bp 3293 of SEQ ID NO: 32 Added Kozak  5 occurs at bp 3327 through bp 3332 of SEQ ID NO: 32 E_GFP 24 occurs at bp 3333 through bp 4052 of SEQ ID NO: 32 SV40 POLYA  8 occurs at bp 4110 through bp 4345 of SEQ ID NO: 32 3′ ITR  9 occurs at bp 4374 through bp 4503 of SEQ ID NO: 32 AMP BACTERIAL 15 BACKBONE occurs at bp 4504 through bp 7122 of SEQ ID NO: 32 Sequence of 32 TM035 Plasmid ctgcgcgctcgctcgctcactgaggccgcccgggcgtcgggc gacctttggtcgcccggcctcagtgagcgagcgagcgcgcag agagggagtggccaactccatcactaggggttcctgcggccg cacgcagcttttgtcctctccctgcttggccttaaccagcca catttctcaactgaccccactcactgcagaggtgaaaactac catgccaggtcctgctggctgggggaggggtgggcaataggc ctggatttgccagagctgccactgtagatgtagtcatattta cgatttcccttcacctcttattaccctggtggtggtggtggg ggggggggggtgctctctcagcaaccccaccccgggatcttg aggagaaagagggcagagaaaagagggaatgggactggccca gatcccagccccacagccgggcttccacatggccgagcagga actccagagcaggagcacacaaaggagggctttgatgcgcct ccagccaggcccaggcctctcccctctcccctttctctctgg gtcttcctttgccccactgagggcctcctgtgagcccgattt aacggaaactgtgggcggtgagaagttccttatgacacacta atcccaacctgctgaccggaccacgcctccagcggagggaac ctctagagctccaggacattcaggtaccaggtagccccaagg aggagctgccgacctggcaggtaagtcaatacctggggcttg cctgggccagggagcccaggactggggtgaggactcagggga gcagggagaccacgtcccaagatgcctgtaaaactgaaacca cctggccattctccaggttgagccagaccaatttgatggcag atttagcaaataaaaatacaggacacccagttaaatgtgaat ttcagatgaacagcaaatacttttttagtattaaaaaagttc acatttaggctcacgcctgtaatcccagcactttgggaggcc gaggcaggcagatcacctgaggtcaggagttcgagaccagcc tggccaacatggtgaaaccccatctccactaaaaataccaaa aattagccaggcgtgctggtgggcacctgtagttccagctac tcaggaggctaaggcaggagaattgcttgaacctgggaggca gaggttgcagtgagctgagatcgcaccattgcactctagcct gggcgacaagaacaaaactccatctcaaaaaaaaaaaaaaaa aaaaagttcacatttaactgggcattctgtatttaattggta atctgagatggcagggaacagcatcagcatggtgtgagggat aggcattttttcattgtgtacagcttgtaaatcagtattttt aaaactcaaagttaatggcttgggcatatttagaaaagagtt gccgcacggacttgaaccctgtattcctaaaatctaggatct tgttctgatggtctgcacaactggctgggggtgtccagccac tgtccctcttgcctgggctccccagggcagttctgtcagcct ctccatttccattcctgttccagcaaaacccaactgatagca cagcagcatttcagcctgtctacctctgtgcccacatacctg gatgtctaccagccagaaaggtggcttagatttggttcctgt gggtggattatggcccccagaacttccctgtgcttgctgggg gtgtggagtggaaagagcaggaaatgggggaccctccgatac tctatgggggtcctccaagtctctttgtgcaagttagggtaa taatcaatatggagctaagaaagagaaggggaactatgcttt agaacaggacactgtgccaggagcattgcagaaattatatgg ttttcacgacagttctttttggtaggtactgttattatcctc agtttgcagatgaggaaactgagacccagaaaggttaaataa cttgctagggtcacacaagtcataactgacaaagcctgattc aaacccaggtctccctaacctttaaggtttctatgacgccag ctctcctagggagtttgtcttcagatgtcttggctctaggtg tcaaaaaaagacttggtgtcaggcaggcataggttcaagtcc caactctgtcacttaccaactgtgactaggtgattgaactga ccatggaacctggtcacatgcaggagcaggatggtgaagggt tcttgaaggcacttaggcaggacatttaggcaggagagaaaa cctggaaacagaagagctgtctccaaaaatacccactgggga agcaggttgtcatgtgggccatgaatgggacctgttctggta accaagcattgcttatgtgtccattacatttcataacacttc catcctactttacagggaacaaccaagactggggttaaatct cacagcctgcaagtggaagagaagaacttgaacccaggtcca acttttgcgccacagcaggctgcctcttggtcctgacaggaa gtcacaacttgggtctgagtactgatccctggctattttttg gctgtgttaccttggacaagtcacttattcctcctcccgttt cctcctatgtaaaatggaaataataatgttgaccctgggtct gagagagtggatttgaaagtacttagtgcatcacaaagcaca gaacacacttccagtctcgtgattatgtacttatgtaactgg tcatcacccatcttgagaatgaatgcattggggaaagggcca tccactaggctgcgaagtttctgagggactccttcgggctgg agaaggatggccacaggagggaggagagattgccttatcctg cagtgatcatgtcattgagaacagagccagattctttttttc ctggcagggccaacttgttttaacatctaaggactgagctat ttgtgtctgtgccctttgtccaagcagtgtttcccaaagtgt agcccaagaaccatctccctcagagccaccaggaagtgcttt aaattgcaggttcctaggccacagcctgcacctgcagagtca gaatcatggaggttgggacccaggcacctgcgtttctaacaa atgcctcgggtgattctgatgcaattgaaagtttgagatcca cagttctgagacaataacagaatggtttttctaacccctgca gccctgacttcctatcctagggaaggggccggctggagaggc caggacagagaaagcagatcccttctttttccaaggactctg tgtcttccataggcaacgaattccccggggatcctctagagt cgaaattcgccaccatggtgagcaagggcgaggagctgttca ccggggtggtgcccatcctggtcgagctggacggcgacgtaa acggccacaagttcagcgtgtccggcgagggcgagggcgatg ccacctacggcaagctgaccctgaagttcatctgcaccaccg gcaagctgcccgtgccctggcccaccctcgtgaccaccctga cctacggcgtgcagtgcttcagccgctaccccgaccacatga agcagcacgacttcttcaagtccgccatgcccgaaggctacg tccaggagcgcaccatcttcttcaaggacgacggcaactaca agacccgcgccgaggtgaagttcgagggcgacaccctggtga accgcatcgagctgaagggcatcgacttcaaggaggacggca acatcctggggcacaagctggagtacaactacaacagccaca acgtctatatcatggccgacaagcagaagaacggcatcaagg tgaacttcaagatccgccacaacatcgaggacggcagcgtgc agctcgccgaccactaccagcagaacacccccatcggcgacg gccccgtgctgctgcccgacaaccactacctgagcacccagt ccgccctgagcaaagaccccaacgagaagcgcgatcacatgg tcctgctggagttcgtgaccgccgccgggatcactctcggca tggacgagctgtacaagtaatagggtaccggtcgacctgcag aagcttgcctcgagcagcgctgctcgagagatctggatcata atcagccataccacatttgtagaggttttacttgctttaaaa aacctcccacacctccccctgaacctgaaacataaaatgaat gcaattgttgttgttaacttgtttattgcagcttataatggt tacaaataaagcaatagcatcacaaatttcacaaataaagca tttttttcactgcattctagttgtggtttgtccaaactcatc aatgtatcttatcatgtctggtaaccacgtgcggaccgagcg gccgcaggaacccctagtgatggagttggccactccctctct gcgcgctcgctcgctcactgaggccgggcgaccaaaggtcgc ccgacgcccgggctttgcccgggcggcctcagtgagcgagcg agcgcgcagctgcctgcaggggcgcctgatgcggtattttct ccttacgcatctgtgcggtatttcacaccgcatacgtcaaag caaccatagtacgcgccctgtagcggcgcattaagcgcggcg ggtgtggtggttacgcgcagcgtgaccgctacacttgccagc gccttagcgcccgctcctttcgctttcttcccttcctttctc gccacgttcgccggctttccccgtcaagctctaaatcggggg ctccctttagggttccgatttagtgctttacggcacctcgac cccaaaaaacttgatttgggtgatggttcacgtagtgggcca tcgccctgatagacggtttttcgccctttgacgttggagtcc acgttctttaatagtggactcttgttccaaactggaacaaca ctcaactctatctcgggctattcttttgatttataagggatt ttgccgatttcggtctattggttaaaaaatgagctgatttaa caaaaatttaacgcgaattttaacaaaatattaacgtttaca attttatggtgcactctcagtacaatctgctctgatgccgca tagttaagccagccccgacacccgccaacacccgctgacgcg ccctgacgggcttgtctgctcccggcatccgcttacagacaa gctgtgaccgtctccgggagctgcatgtgtcagaggttttca ccgtcatcaccgaaacgcgcgagacgaaagggcctcgtgata cgcctatttttataggttaatgtcatgataataatggtttct tagacgtcaggtggcacttttcggggaaatgtgcgcggaacc cctatttgtttatttttctaaatacattcaaatatgtatccg ctcatgagacaataaccctgataaatgcttcaataatattga aaaaggaagagtatgagtattcaacatttccgtgtcgccctt attcccttttttgcggcattttgccttcctgtttttgctcac ccagaaacgctggtgaaagtaaaagatgctgaagatcagttg ggtgcacgagtgggttacatcgaactggatctcaacagcggt aagatccttgagagttttcgccccgaagaacgttttccaatg atgagcacttttaaagttctgctatgtggcgcggtattatcc cgtattgacgccgggcaagagcaactcggtcgccgcatacac tattctcagaatgacttggttgagtactcaccagtcacagaa aagcatcttacggatggcatgacagtaagagaattatgcagt gctgccataaccatgagtgataacactgcggccaacttactt ctgacaacgatcggaggaccgaaggagctaaccgcttttttg cacaacatgggggatcatgtaactcgccttgatcgttgggaa ccggagctgaatgaagccataccaaacgacgagcgtgacacc acgatgcctgtagcaatggcaacaacgttgcgcaaactatta actggcgaactacttactctagcttcccggcaacaattaata gactggatggaggcggataaagttgcaggaccacttctgcgc tcggcccttccggctggctggtttattgctgataaatctgga gccggtgagcgtgggtctcgcggtatcattgcagcactgggg ccagatggtaagccctcccgtatcgtagttatctacacgacg gggagtcaggcaactatggatgaacgaaatagacagatcgct gagataggtgcctcactgattaagcattggtaactgtcagac caagtttactcatatatactttagattgatttaaaacttcat ttttaatttaaaaggatctaggtgaagatcctttttgataat ctcatgaccaaaatcccttaacgtgagttttcgttccactga gcgtcagaccccgtagaaaagatcaaaggatcttcttgaaat cctttttttctgcgcgtaatctgctgcttgcaaacaaaaaaa ccaccgctaccagcggtggtttgtttgccggatcaagagcta ccaactctttttccgaaggtaactggcttcagcagagcgcag ataccaaatactgttcttctagtgtagccgtagttaggccac cacttcaagaactctgtagcaccgcctacatacctcgctctg ctaatcctgttaccagtggctgctgccagtggcgataagtcg tgtcttaccgggttggactcaagacgatagttaccggataag gcgcagcggtcgggctgaacggggggttcgtgcacacagccc agcttggagcgaacgacctacaccgaactgagatacctacag cgtgagctatgagaaagcgccacgcttcccgaagggagaaag gcggacaggtatccggtaagcggcagggtcggaacaggagag cgcacgagggagcttccagggggaaacgcctggtatctttat agtcctgtcgggtttcgccacctctgacttgagcgtcgattt ttgtgatgctcgtcaggggggcggagcctatggaaaaacgcc agcaacgcggcctttttacggttcctggccttttgctggcct tttgctcacatgtcctgcaggcag GENE CASSETTE 57 OF PLASMID ctgcgcgctcgctcgctcactgaggccgcccgggcgtcgggc TM035 OCCURS AT gacctttggtcgcccggcctcagtgagcgagcgagcgcgcag BP 1 THROUGH agagggagtggccaactccatcactaggggttcctgcggccg 4503 OF SEQ ID cacgcagcttttgtcctctccctgcttggccttaaccagcca NO: 32 catttctcaactgaccccactcactgcagaggtgaaaactac catgccaggtcctgctggctgggggaggggtgggcaataggc ctggatttgccagagctgccactgtagatgtagtcatattta cgatttcccttcacctcttattaccctggtggtggtggtggg ggggggggggtgctctctcagcaaccccaccccgggatcttg aggagaaagagggcagagaaaagagggaatgggactggccca gatcccagccccacagccgggcttccacatggccgagcagga actccagagcaggagcacacaaaggagggctttgatgcgcct ccagccaggcccaggcctctcccctctcccctttctctctgg gtcttcctttgccccactgagggcctcctgtgagcccgattt aacggaaactgtgggcggtgagaagttccttatgacacacta atcccaacctgctgaccggaccacgcctccagcggagggaac ctctagagctccaggacattcaggtaccaggtagccccaagg aggagctgccgacctggcaggtaagtcaatacctggggcttg cctgggccagggagcccaggactggggtgaggactcagggga gcagggagaccacgtcccaagatgcctgtaaaactgaaacca cctggccattctccaggttgagccagaccaatttgatggcag atttagcaaataaaaatacaggacacccagttaaatgtgaat ttcagatgaacagcaaatacttttttagtattaaaaaagttc acatttaggctcacgcctgtaatcccagcactttgggaggcc gaggcaggcagatcacctgaggtcaggagttcgagaccagcc tggccaacatggtgaaaccccatctccactaaaaataccaaa aattagccaggcgtgctggtgggcacctgtagttccagctac tcaggaggctaaggcaggagaattgcttgaacctgggaggca gaggttgcagtgagctgagatcgcaccattgcactctagcct gggcgacaagaacaaaactccatctcaaaaaaaaaaaaaaaa aaaaagttcacatttaactgggcattctgtatttaattggta atctgagatggcagggaacagcatcagcatggtgtgagggat aggcattttttcattgtgtacagcttgtaaatcagtattttt aaaactcaaagttaatggcttgggcatatttagaaaagagtt gccgcacggacttgaaccctgtattcctaaaatctaggatct tgttctgatggtctgcacaactggctgggggtgtccagccac tgtccctcttgcctgggctccccagggcagttctgtcagcct ctccatttccattcctgttccagcaaaacccaactgatagca cagcagcatttcagcctgtctacctctgtgcccacatacctg gatgtctaccagccagaaaggtggcttagatttggttcctgt gggtggattatggcccccagaacttccctgtgcttgctgggg gtgtggagtggaaagagcaggaaatgggggaccctccgatac tctatgggggtcctccaagtctctttgtgcaagttagggtaa taatcaatatggagctaagaaagagaaggggaactatgcttt agaacaggacactgtgccaggagcattgcagaaattatatgg ttttcacgacagttctttttggtaggtactgttattatcctc agtttgcagatgaggaaactgagacccagaaaggttaaataa cttgctagggtcacacaagtcataactgacaaagcctgattc aaacccaggtctccctaacctttaaggtttctatgacgccag ctctcctagggagtttgtcttcagatgtcttggctctaggtg tcaaaaaaagacttggtgtcaggcaggcataggttcaagtcc caactctgtcacttaccaactgtgactaggtgattgaactga ccatggaacctggtcacatgcaggagcaggatggtgaagggt tcttgaaggcacttaggcaggacatttaggcaggagagaaaa cctggaaacagaagagctgtctccaaaaatacccactgggga agcaggttgtcatgtgggccatgaatgggacctgttctggta accaagcattgcttatgtgtccattacatttcataacacttc catcctactttacagggaacaaccaagactggggttaaatct cacagcctgcaagtggaagagaagaacttgaacccaggtcca acttttgcgccacagcaggctgcctcttggtcctgacaggaa gtcacaacttgggtctgagtactgatccctggctattttttg gctgtgttaccttggacaagtcacttattcctcctcccgttt cctcctatgtaaaatggaaataataatgttgaccctgggtct gagagagtggatttgaaagtacttagtgcatcacaaagcaca gaacacacttccagtctcgtgattatgtacttatgtaactgg tcatcacccatcttgagaatgaatgcattggggaaagggcca tccactaggctgcgaagtttctgagggactccttcgggctgg agaaggatggccacaggagggaggagagattgccttatcctg cagtgatcatgtcattgagaacagagccagattctttttttc ctggcagggccaacttgttttaacatctaaggactgagctat ttgtgtctgtgccctttgtccaagcagtgtttcccaaagtgt agcccaagaaccatctccctcagagccaccaggaagtgcttt aaattgcaggttcctaggccacagcctgcacctgcagagtca gaatcatggaggttgggacccaggcacctgcgtttctaacaa atgcctcgggtgattctgatgcaattgaaagtttgagatcca cagttctgagacaataacagaatggtttttctaacccctgca gccctgacttcctatcctagggaaggggccggctggagaggc caggacagagaaagcagatcccttctttttccaaggactctg tgtcttccataggcaacgaattccccggggatcctctagagt cgaaattcgccaccatggtgagcaagggcgaggagctgttca ccggggtggtgcccatcctggtcgagctggacggcgacgtaa acggccacaagttcagcgtgtccggcgagggcgagggcgatg ccacctacggcaagctgaccctgaagttcatctgcaccaccg gcaagctgcccgtgccctggcccaccctcgtgaccaccctga cctacggcgtgcagtgcttcagccgctaccccgaccacatga agcagcacgacttcttcaagtccgccatgcccgaaggctacg tccaggagcgcaccatcttcttcaaggacgacggcaactaca agacccgcgccgaggtgaagttcgagggcgacaccctggtga accgcatcgagctgaagggcatcgacttcaaggaggacggca acatcctggggcacaagctggagtacaactacaacagccaca acgtctatatcatggccgacaagcagaagaacggcatcaagg tgaacttcaagatccgccacaacatcgaggacggcagcgtgc agctcgccgaccactaccagcagaacacccccatcggcgacg gccccgtgctgctgcccgacaaccactacctgagcacccagt ccgccctgagcaaagaccccaacgagaagcgcgatcacatgg tcctgctggagttcgtgaccgccgccgggatcactctcggca tggacgagctgtacaagtaatagggtaccggtcgacctgcag aagcttgcctcgagcagcgctgctcgagagatctggatcata atcagccataccacatttgtagaggttttacttgctttaaaa aacctcccacacctccccctgaacctgaaacataaaatgaat gcaattgttgttgttaacttgtttattgcagcttataatggt tacaaataaagcaatagcatcacaaatttcacaaataaagca tttttttcactgcattctagttgtggtttgtccaaactcatc aatgtatcttatcatgtctggtaaccacgtgcggaccgagcg gccgcaggaacccctagtgatggagttggccactccctctct gcgcgctcgctcgctcactgaggccgggcgaccaaaggtcgc ccgacgcccgggctttgcccgggcggcctcagtgagcgagcg agcgcgcag Plasmid AG012 Composition 5′ ITR  2 occurs @ bp 1 through bp 119 of SEQ ID NO: 33 SYNUCLEIN 13 INTRONIC occurs @ bp 148 through bp 2601 of SEQ ID SEQUENCE AS NO: 33 STUFFER SEQUENCE SV40 POLYA  8 occurs @ bp 2640 through bp 2875 of SEQ ID NO: 33 RLBP1 INTRONIC 14 SEQUENCE AS occurs at bp 2883 through bp 4385 of SEQ STUFFER ID NO: 33 SEQUENCE 3′ ITR  9 occurs at bp 4414 through bp 4543 of SEQ ID NO: 33 AMP BACTERIAL 15 BACKBONE occurs at bp 4544 through bp 7162 of SEQ ID NO: 33 Sequence of 33 AG012 Plasmid ctgcgcgctcgctcgctcactgaggccgcccgggcgtcgggc gacctttggtcgcccggcctcagtgagcgagcgagcgcgcag agagggagtggccaactccatcactaggggttcctgcggccg cacgcgtgacgtcgtttaaacgggccccggtgttatctcatt cttttttctcctctgtaagttgacatgtgatgtgggaacaaa ggggataaagtcattattttgtgctaaaatcgtaattggaga ggacctcctgttagctgggctttcttctatttattgtggtgg ttactggagttccttcttctagttttaggatatatatatata ttttttttttttctttccctgaagatataataatatatatac ttctgaagattgagatttttaaattagttgtattgaaaacta gctaatcagcaatttaaggctagcttgagacttatgtcttga atttgtttttgtaggctccaaaaccaaggagggagtggtgca tggtgtggcaacaggtaagctccattgtgcttatatccaaag atgatatttaaagtatctagtgattagtgtggcccagtattc aagattcctatgaaattgtaaaacaatcactgagcattctaa gaacatatcagtcttattgaaactgaattctttataaagtat ttttaaaaaggtaaatattgattataaataaaaaatatactt gccaagaataatgagggctttgaattgataagctatgtttaa tttatagtaagtgggcatttaaatattctgaccaaaaatgta ttgacaaactgctgacaaaaataaaatgtgaatattgccata attttaaaaaaagagtaaaatttctgttgattacagtaaaat attttgaccttaaattatgttgattacaatattcctttgata attcagagtgcatttcaggaaacacccttggacagtcagtaa attgtttattgtatttatctttgtattgttatggtatagcta tttgtacaaatattattgtgcaattattacatttctgattat attattcatttggcctaaatttaccaagaatttgaacaagtc aattaggtttacaatcaagaaatatcaaaaatgatgaaaagg atgataatcatcatcagatgttgaggaagatgacgatgagag tgccagaaatagagaaatcaaaggagaaccaaaatttaacaa attaaaagcccacagacttgctgtaattaagttttctgttgt aagtactccacgtttcctggcagatgtggtgaagcaaaagat ataatcagaaatataatttatatgatcggaaagcattaaaca caatagtgcctatacaaataaaatgttcctatcactgacttc taaaatggaaatgaggacaatgatatgggaatcttaatacag tgttgtggataggactaaaaacacaggagtcagatcttcttg gttcaacttcctgcttactccttaccagctgtgtgttttttg caaggttcttcacctctatgtgatttagcttcctcatctata aaataattcagtgaattaatgtacacaaaacatctggaaaac aaaagcaaacaatatgtattttataagtgttacttatagttt tatagtgaactttcttgtgcaacatttttacaactagtggag aaaaatatttctttaaatgaatacttttgatttaaaaatcag agtgtaaaaataaaacagactcctttgaaactagttctgtta gaagttaattgtgcacctttaatgggctctgttgcaatccaa cagagaagtagttaagtaagtggactatgatggcttctaggg acctcctataaatatgatattgtgaagcatgattataataag aactagataacagacaggtggagactccactatctgaagagg gtcaacctagatgaatggtgttccatttagtagttgaggaag aacccatgaggtttagaaagcagacaagcatgtggcaagttc tggagtcagtggtaaaaattaaagaacccaactattactgtc acctaatgatctaatggagactgtggagatgggctgcatttt tttaatcttctccagaatgccaaaatgtaaacacatatctgt gtgtgtgtgtgtgtgtgtgtgtgtgtgtgagagagagagaga gagagagagagactgaagtttgtacaattagacattttataa aatgttttctgaaggacagtggctcacaatcttaagtttcta acattgtacaatgttgggagactttgtatactttattttctc tttagcatattaaggaatctgagatgtcctacagtaaagaaa tttgcattacatagttaaaatcagggttattcaaactttttg attattgaaacctttcttcattagttactagggttgaatgaa actagtgttccacagaaaactatgggaaatgttgctaggcag taaggacatggtgatttcagcatgtgcaatatttacagcgat tgcacccatggaccaccctggcagtagtgaaataaccaaaaa tgctgtcataactagtatggctatgagaaacacattgggcag aagcttgcctcgagcagcgctgctcgagagatctggatcata atcagccataccacatttgtagaggttttacttgctttaaaa aacctcccacacctccccctgaacctgaaacataaaatgaat gcaattgttgttgttaacttgtttattgcagcttataatggt tacaaataaagcaatagcatcacaaatttcacaaataaagca tttttttcactgcattctagttgtggtttgtccaaactcatc aatgtatcttatcatgtctggtaaccattctccaggttgagc cagaccaatttgatggtagatttagcaaataaaaatacagga cacccagttaaatgtgaatttccgatgaacagcaaatacttt tttagtattaaaaaagttcacatttaggctcacgcctgtaat cccagcactttgggaggccgaggcaggcagatcacctgaggt caggagttcgagaccagcctggccaacatggtgaaaccccat ctccactaaaaataccaaaaattagccaggcgtgctggtggg cacctgtagttccagctactcaggaggctaaggcaggagaat tgcttgaacctgggaggcagaggttgcagtgagctgagatcg caccattgcactctagcctgggcgacaagaacaaaactccat ctcaaaaaaaaaaaaaaaaaaaaagttcacatttaactgggc attctgtatttaattggtaatctgagatggcagggaacagca tcagcatggtgtgagggataggcattttttcattgtgtacag cttgtaaatcagtatttttaaaactcaaagttaatggcttgg gcatatttagaaaagagttgccgcacggacttgaaccctgta ttcctaaaatctaggatcttgttctgatggtctgcacaactg gctgggggtgtccagccactgtccctcttgcctgggctcccc agggcagttctgtcagcctctccatttccattcctgttccag caaaacccaactgatagcacagcagcatttcagcctgtctac ctctgtgcccacatacctggatgtctaccagccagaaaggtg gcttagatttggttcctgtgggtggattatggcccccagaac ttccctgtgcttgctgggggtgtggagtggaaagagcaggaa atgggggaccctccgatactctatgggggtcctccaagtctc tttgtgcaagttagggtaataatcaatatggagctaagaaag agaaggggaactatgctttagaacaggacactgtgccaggag cattgcagaaattatatggttttcacgacagttctttttggt aggtactgttattatcctcagtttgcagatgaggaaactgag acccagaaaggttaaataacttgctagggtcacacaagtcat aactgacaaagcctgattcaaacccaggtctccctaaccttt aaggtttctatgacgccagctctcctagggagtttgtcttca gatgtcttggctctaggtgtcaaaaaaagacttggtgtcagg caggcataggttcaagtcccaactctgtcacttaccaactgt gactaggtgattgaactgaccatggaacctggtcacatgcag gagcaggatggtgaagggttcttgaaggcacttaggcaggac atttaggcaggagagaaaacctggaaacagaagagctgtctc caaaaatacccactggggaagcaggttgtcatgtgggccatg aatgggacctgttctggggtaaccacgtgcggaccgagcggc cgcaggaacccctagtgatggagttggccactccctctctgc gcgctcgctcgctcactgaggccgggcgaccaaaggtcgccc gacgcccgggctttgcccgggcggcctcagtgagcgagcgag cgcgcagctgcctgcaggggcgcctgatgcggtattttctcc ttacgcatctgtgcggtatttcacaccgcatacgtcaaagca accatagtacgcgccctgtagcggcgcattaagcgcggcggg tgtggtggttacgcgcagcgtgaccgctacacttgccagcgc cttagcgcccgctcctttcgctttcttcccttcctttctcgc cacgttcgccggctttccccgtcaagctctaaatcgggggct ccctttagggttccgatttagtgctttacggcacctcgaccc caaaaaacttgatttgggtgatggttcacgtagtgggccatc gccctgatagacggtttttcgccctttgacgttggagtccac gttctttaatagtggactcttgttccaaactggaacaacact caactctatctcgggctattcttttgatttataagggatttt gccgatttcggtctattggttaaaaaatgagctgatttaaca aaaatttaacgcgaattttaacaaaatattaacgtttacaat tttatggtgcactctcagtacaatctgctctgatgccgcata gttaagccagccccgacacccgccaacacccgctgacgcgcc ctgacgggcttgtctgctcccggcatccgcttacagacaagc tgtgaccgtctccgggagctgcatgtgtcagaggttttcacc gtcatcaccgaaacgcgcgagacgaaagggcctcgtgatacg cctatttttataggttaatgtcatgataataatggtttctta gacgtcaggtggcacttttcggggaaatgtgcgcggaacccc tatttgtttatttttctaaatacattcaaatatgtatccgct catgagacaataaccctgataaatgcttcaataatattgaaa aaggaagagtatgagtattcaacatttccgtgtcgcccttat tcccttttttgcggcattttgccttcctgtttttgctcaccc agaaacgctggtgaaagtaaaagatgctgaagatcagttggg tgcacgagtgggttacatcgaactggatctcaacagcggtaa gatccttgagagttttcgccccgaagaacgttttccaatgat gagcacttttaaagttctgctatgtggcgcggtattatcccg tattgacgccgggcaagagcaactcggtcgccgcatacacta ttctcagaatgacttggttgagtactcaccagtcacagaaaa gcatcttacggatggcatgacagtaagagaattatgcagtgc tgccataaccatgagtgataacactgcggccaacttacttct gacaacgatcggaggaccgaaggagctaaccgcttttttgca caacatgggggatcatgtaactcgccttgatcgttgggaacc ggagctgaatgaagccataccaaacgacgagcgtgacaccac gatgcctgtagcaatggcaacaacgttgcgcaaactattaac tggcgaactacttactctagcttcccggcaacaattaataga ctggatggaggcggataaagttgcaggaccacttctgcgctc ggcccttccggctggctggtttattgctgataaatctggagc cggtgagcgtgggtctcgcggtatcattgcagcactggggcc agatggtaagccctcccgtatcgtagttatctacacgacggg gagtcaggcaactatggatgaacgaaatagacagatcgctga gataggtgcctcactgattaagcattggtaactgtcagacca agtttactcatatatactttagattgatttaaaacttcattt ttaatttaaaaggatctaggtgaagatcctttttgataatct catgaccaaaatcccttaacgtgagttttcgttccactgagc gtcagaccccgtagaaaagatcaaaggatcttcttgaaatcc tttttttctgcgcgtaatctgctgcttgcaaacaaaaaaacc accgctaccagcggtggtttgtttgccggatcaagagctacc aactctttttccgaaggtaactggcttcagcagagcgcagat accaaatactgttcttctagtgtagccgtagttaggccacca cttcaagaactctgtagcaccgcctacatacctcgctctgct aatcctgttaccagtggctgctgccagtggcgataagtcgtg tcttaccgggttggactcaagacgatagttaccggataaggc gcagcggtcgggctgaacggggggttcgtgcacacagcccag cttggagcgaacgacctacaccgaactgagatacctacagcg tgagctatgagaaagcgccacgcttcccgaagggagaaaggc ggacaggtatccggtaagcggcagggtcggaacaggagagcg cacgagggagcttccagggggaaacgcctggtatctttatag tcctgtcgggtttcgccacctctgacttgagcgtcgattttt gtgatgctcgtcaggggggcggagcctatggaaaaacgccag caacgcggcctttttacggttcctggccttttgctggccttt tgctcacatgtcctgcaggcag INSERT OF 58 PLASMID AG012 ctgcgcgctcgctcgctcactgaggccgcccgggcgtcgggc OCCURS AT BP 1 gacctttggtcgcccggcctcagtgagcgagcgagcgcgcag THROUGH 4543 OF agagggagtggccaactccatcactaggggttcctgcggccg SEQ ID NO: 33 cacgcgtgacgtcgtttaaacgggccccggtgttatctcatt (USED AS cttttttctcctctgtaagttgacatgtgatgtgggaacaaa NEGATIVE ggggataaagtcattattttgtgctaaaatcgtaattggaga CONTROL FOR ggacctcctgttagctgggctttcttctatttattgtggtgg GENE CASSETTE) ttactggagttccttcttctagttttaggatatatatatata ttttttttttttctttccctgaagatataataatatatatac ttctgaagattgagatttttaaattagttgtattgaaaacta gctaatcagcaatttaaggctagcttgagacttatgtcttga atttgtttttgtaggctccaaaaccaaggagggagtggtgca tggtgtggcaacaggtaagctccattgtgcttatatccaaag atgatatttaaagtatctagtgattagtgtggcccagtattc aagattcctatgaaattgtaaaacaatcactgagcattctaa gaacatatcagtcttattgaaactgaattctttataaagtat ttttaaaaaggtaaatattgattataaataaaaaatatactt gccaagaataatgagggctttgaattgataagctatgtttaa tttatagtaagtgggcatttaaatattctgaccaaaaatgta ttgacaaactgctgacaaaaataaaatgtgaatattgccata attttaaaaaaagagtaaaatttctgttgattacagtaaaat attttgaccttaaattatgttgattacaatattcctttgata attcagagtgcatttcaggaaacacccttggacagtcagtaa attgtttattgtatttatctttgtattgttatggtatagcta tttgtacaaatattattgtgcaattattacatttctgattat attattcatttggcctaaatttaccaagaatttgaacaagtc aattaggtttacaatcaagaaatatcaaaaatgatgaaaagg atgataatcatcatcagatgttgaggaagatgacgatgagag tgccagaaatagagaaatcaaaggagaaccaaaatttaacaa attaaaagcccacagacttgctgtaattaagttttctgttgt aagtactccacgtttcctggcagatgtggtgaagcaaaagat ataatcagaaatataatttatatgatcggaaagcattaaaca caatagtgcctatacaaataaaatgttcctatcactgacttc taaaatggaaatgaggacaatgatatgggaatcttaatacag tgttgtggataggactaaaaacacaggagtcagatcttcttg gttcaacttcctgcttactccttaccagctgtgtgttttttg caaggttcttcacctctatgtgatttagcttcctcatctata aaataattcagtgaattaatgtacacaaaacatctggaaaac aaaagcaaacaatatgtattttataagtgttacttatagttt tatagtgaactttcttgtgcaacatttttacaactagtggag aaaaatatttctttaaatgaatacttttgatttaaaaatcag agtgtaaaaataaaacagactcctttgaaactagttctgtta gaagttaattgtgcacctttaatgggctctgttgcaatccaa cagagaagtagttaagtaagtggactatgatggcttctaggg acctcctataaatatgatattgtgaagcatgattataataag aactagataacagacaggtggagactccactatctgaagagg gtcaacctagatgaatggtgttccatttagtagttgaggaag aacccatgaggtttagaaagcagacaagcatgtggcaagttc tggagtcagtggtaaaaattaaagaacccaactattactgtc acctaatgatctaatggagactgtggagatgggctgcatttt tttaatcttctccagaatgccaaaatgtaaacacatatctgt gtgtgtgtgtgtgtgtgtgtgtgtgtgtgagagagagagaga gagagagagagactgaagtttgtacaattagacattttataa aatgttttctgaaggacagtggctcacaatcttaagtttcta acattgtacaatgttgggagactttgtatactttattttctc tttagcatattaaggaatctgagatgtcctacagtaaagaaa tttgcattacatagttaaaatcagggttattcaaactttttg attattgaaacctttcttcattagttactagggttgaatgaa actagtgttccacagaaaactatgggaaatgttgctaggcag taaggacatggtgatttcagcatgtgcaatatttacagcgat tgcacccatggaccaccctggcagtagtgaaataaccaaaaa tgctgtcataactagtatggctatgagaaacacattgggcag aagcttgcctcgagcagcgctgctcgagagatctggatcata atcagccataccacatttgtagaggttttacttgctttaaaa aacctcccacacctccccctgaacctgaaacataaaatgaat gcaattgttgttgttaacttgtttattgcagcttataatggt tacaaataaagcaatagcatcacaaatttcacaaataaagca tttttttcactgcattctagttgtggtttgtccaaactcatc aatgtatcttatcatgtctggtaaccattctccaggttgagc cagaccaatttgatggtagatttagcaaataaaaatacagga cacccagttaaatgtgaatttccgatgaacagcaaatacttt tttagtattaaaaaagttcacatttaggctcacgcctgtaat cccagcactttgggaggccgaggcaggcagatcacctgaggt caggagttcgagaccagcctggccaacatggtgaaaccccat ctccactaaaaataccaaaaattagccaggcgtgctggtggg cacctgtagttccagctactcaggaggctaaggcaggagaat tgcttgaacctgggaggcagaggttgcagtgagctgagatcg caccattgcactctagcctgggcgacaagaacaaaactccat ctcaaaaaaaaaaaaaaaaaaaaagttcacatttaactgggc attctgtatttaattggtaatctgagatggcagggaacagca tcagcatggtgtgagggataggcattttttcattgtgtacag cttgtaaatcagtatttttaaaactcaaagttaatggcttgg gcatatttagaaaagagttgccgcacggacttgaaccctgta ttcctaaaatctaggatcttgttctgatggtctgcacaactg gctgggggtgtccagccactgtccctcttgcctgggctcccc agggcagttctgtcagcctctccatttccattcctgttccag caaaacccaactgatagcacagcagcatttcagcctgtctac ctctgtgcccacatacctggatgtctaccagccagaaaggtg gcttagatttggttcctgtgggtggattatggcccccagaac ttccctgtgcttgctgggggtgtggagtggaaagagcaggaa atgggggaccctccgatactctatgggggtcctccaagtctc tttgtgcaagttagggtaataatcaatatggagctaagaaag agaaggggaactatgctttagaacaggacactgtgccaggag cattgcagaaattatatggttttcacgacagttctttttggt aggtactgttattatcctcagtttgcagatgaggaaactgag acccagaaaggttaaataacttgctagggtcacacaagtcat aactgacaaagcctgattcaaacccaggtctccctaaccttt aaggtttctatgacgccagctctcctagggagtttgtcttca gatgtcttggctctaggtgtcaaaaaaagacttggtgtcagg caggcataggttcaagtcccaactctgtcacttaccaactgt gactaggtgattgaactgaccatggaacctggtcacatgcag gagcaggatggtgaagggttcttgaaggcacttaggcaggac atttaggcaggagagaaaacctggaaacagaagagctgtctc caaaaatacccactggggaagcaggttgtcatgtgggccatg aatgggacctgttctggggtaaccacgtgcggaccgagcggc cgcaggaacccctagtgatggagttggccactccctctctgc gcgctcgctcgctcactgaggccgggcgaccaaaggtcgccc gacgcccgggctttgcccgggcggcctcagtgagcgagcgag cgcgcag Plasmid AG004 Composition 5′ ITR  2 occurs @ bp 1 through bp 119 of SEQ ID NO: 34 Human RPE65 11 Promoter occurs @ bp 134 through bp 1718 of SEQ ID NO: 34 Added Kozak  5 occurs @ bp 1752 through 1757 of of SEQ ID NO: 34 E-GFP 24 occurs @ bp 1758 through bp 2477 of SEQ ID NO: 34 SV40 POLYA  8 occurs at bp 2535 through bp 2770 of SEQ ID NO: 34 RLBP1 INTRONIC 14 SEQUENCE AS occurs at bp 2778 through bp 4280 of SEQ STUFFER ID NO: 34 SEQUENCE 3′ ITR  9 occurs at bp 4309 through bp 4438 of SEQ ID NO: 34 AMP BACTERIAL 15 BACKBONE occurs at bp 4439 through bp 7057 of SEQ ID NO: 34 Sequence of 34 plasmid AG004 ctgcgcgctcgctcgctcactgaggccgcccgggcgtcgggc gacctttggtcgcccggcctcagtgagcgagcgagcgcgcag agagggagtggccaactccatcactaggggttcctgcggccg cacgcgttacgtaatatttattgaagtttaatattgtgtttg tgatacagaagtatttgctttaattctaaataaaaattttat gcttttattgctggtttaagaagatttggattatccttgtac tttgaggagaagtttcttatttgaaatattttggaaacaggt cttttaatgtggaaagatagatattaatctcctcttctatta ctctccaagatccaacaaaagtgattataccccccaaaatat gatggtagtatcttatactaccatcattttataggcataggg ctcttagctgcaaataatggaactaactctaataaagcagaa cgcaaatattgtaaatattagagagctaacaatctctgggat ggctaaaggatggagcttggaggctacccagccagtaacaat attccgggctccactgttgaatggagacactacaactgcctt ggatgggcagagatattatggatgctaagccccaggtgctac cattaggacttctaccactgtccctaacgggtggagcccatc acatgcctatgccctcactgtaaggaaatgaagctactgttg tatatcttgggaagcacttggattaattgttatacagttttg ttgaagaagacccctagggtaagtagccataactgcacacta aatttaaaattgttaatgagtttctcaaaaaaaatgttaagg ttgttagctggtatagtatatatcttgcctgttttccaagga cttctttgggcagtaccttgtctgtgctggcaagcaactgag acttaatgaaagagtattggagatatgaatgaattgatgctg tatactctcagagtgccaaacatataccaatggacaagaagg tgaggcagagagcagacaggcattagtgacaagcaaagatat gcagaatttcattctcagcaaatcaaaagtcctcaacctggt tggaagaatattggcactgaatggtatcaataaggttgctag agagggttagaggtgcacaatgtgcttccataacattttata cttctccaatcttagcactaatcaaacatggttgaatacttt gtttactataactcttacagagttataagatctgtgaagaca gggacagggacaatacccatctctgtctggttcataggtggt atgtaatagatatttttaaaaataagtgagttaatgaatgag ggtgagaatgaaggcacagaggtattagggggaggtgggccc cagagaatggtgccaaggtccagtggggtgactgggatcagc tcaggcctgacgctggccactcccacctagctcctttctttc taatctgttctcattctccttgggaaggattgaggtctctgg aaaacagccaaacaactgttatgggaacagcaagcccaaata aagccaagcatcagggggatctgagagctgaaagcaacttct gttccccctccctcagctgaaggggtggggaagggctcccaa agccataactccttttaagggatttagaaggcataaaaaggc ccctggctgagaacttccttcttcattctgcagttggtgaat tccccggggatcctctagagtcgaaattcgccaccatggtga gcaagggcgaggagctgttcaccggggtggtgcccatcctgg tcgagctggacggcgacgtaaacggccacaagttcagcgtgt ccggcgagggcgagggcgatgccacctacggcaagctgaccc tgaagttcatctgcaccaccggcaagctgcccgtgccctggc ccaccctcgtgaccaccctgacctacggcgtgcagtgcttca gccgctaccccgaccacatgaagcagcacgacttcttcaagt ccgccatgcccgaaggctacgtccaggagcgcaccatcttct tcaaggacgacggcaactacaagacccgcgccgaggtgaagt tcgagggcgacaccctggtgaaccgcatcgagctgaagggca tcgacttcaaggaggacggcaacatcctggggcacaagctgg agtacaactacaacagccacaacgtctatatcatggccgaca agcagaagaacggcatcaaggtgaacttcaagatccgccaca acatcgaggacggcagcgtgcagctcgccgaccactaccagc agaacacccccatcggcgacggccccgtgctgctgcccgaca accactacctgagcacccagtccgccctgagcaaagacccca acgagaagcgcgatcacatggtcctgctggagttcgtgaccg ccgccgggatcactctcggcatggacgagctgtacaagtaat agggtaccggtcgacctgcagaagcttgcctcgagcagcgct gctcgagagatctggatcataatcagccataccacatttgta gaggttttacttgctttaaaaaacctcccacacctccccctg aacctgaaacataaaatgaatgcaattgttgttgttaacttg tttattgcagcttataatggttacaaataaagcaatagcatc acaaatttcacaaataaagcatttttttcactgcattctagt tgtggtttgtccaaactcatcaatgtatcttatcatgtctgg taaccattctccaggttgagccagaccaatttgatggtagat ttagcaaataaaaatacaggacacccagttaaatgtgaattt ccgatgaacagcaaatacttttttagtattaaaaaagttcac atttaggctcacgcctgtaatcccagcactttgggaggccga ggcaggcagatcacctgaggtcaggagttcgagaccagcctg gccaacatggtgaaaccccatctccactaaaaataccaaaaa ttagccaggcgtgctggtgggcacctgtagttccagctactc aggaggctaaggcaggagaattgcttgaacctgggaggcaga ggttgcagtgagctgagatcgcaccattgcactctagcctgg gcgacaagaacaaaactccatctcaaaaaaaaaaaaaaaaaa aaagttcacatttaactgggcattctgtatttaattggtaat ctgagatggcagggaacagcatcagcatggtgtgagggatag gcattttttcattgtgtacagcttgtaaatcagtatttttaa aactcaaagttaatggcttgggcatatttagaaaagagttgc cgcacggacttgaaccctgtattcctaaaatctaggatcttg ttctgatggtctgcacaactggctgggggtgtccagccactg tccctcttgcctgggctccccagggcagttctgtcagcctct ccatttccattcctgttccagcaaaacccaactgatagcaca gcagcatttcagcctgtctacctctgtgcccacatacctgga tgtctaccagccagaaaggtggcttagatttggttcctgtgg gtggattatggcccccagaacttccctgtgcttgctgggggt gtggagtggaaagagcaggaaatgggggaccctccgatactc tatgggggtcctccaagtctctttgtgcaagttagggtaata atcaatatggagctaagaaagagaaggggaactatgctttag aacaggacactgtgccaggagcattgcagaaattatatggtt ttcacgacagttctttttggtaggtactgttattatcctcag tttgcagatgaggaaactgagacccagaaaggttaaataact tgctagggtcacacaagtcataactgacaaagcctgattcaa acccaggtctccctaacctttaaggtttctatgacgccagct ctcctagggagtttgtcttcagatgtcttggctctaggtgtc aaaaaaagacttggtgtcaggcaggcataggttcaagtccca actctgtcacttaccaactgtgactaggtgattgaactgacc atggaacctggtcacatgcaggagcaggatggtgaagggttc ttgaaggcacttaggcaggacatttaggcaggagagaaaacc tggaaacagaagagctgtctccaaaaatacccactggggaag caggttgtcatgtgggccatgaatgggacctgttctggggta accacgtgcggaccgagcggccgcaggaacccctagtgatgg agttggccactccctctctgcgcgctcgctcgctcactgagg ccgggcgaccaaaggtcgcccgacgcccgggctttgcccggg cggcctcagtgagcgagcgagcgcgcagctgcctgcaggggc gcctgatgcggtattttctccttacgcatctgtgcggtattt cacaccgcatacgtcaaagcaaccatagtacgcgccctgtag cggcgcattaagcgcggcgggtgtggtggttacgcgcagcgt gaccgctacacttgccagcgccttagcgcccgctcctttcgc tttcttcccttcctttctcgccacgttcgccggctttccccg tcaagctctaaatcgggggctccctttagggttccgatttag tgctttacggcacctcgaccccaaaaaacttgatttgggtga tggttcacgtagtgggccatcgccctgatagacggtttttcg ccctttgacgttggagtccacgttctttaatagtggactctt gttccaaactggaacaacactcaactctatctcgggctattc ttttgatttataagggattttgccgatttcggtctattggtt aaaaaatgagctgatttaacaaaaatttaacgcgaattttaa caaaatattaacgtttacaattttatggtgcactctcagtac aatctgctctgatgccgcatagttaagccagccccgacaccc gccaacacccgctgacgcgccctgacgggcttgtctgctccc ggcatccgcttacagacaagctgtgaccgtctccgggagctg catgtgtcagaggttttcaccgtcatcaccgaaacgcgcgag acgaaagggcctcgtgatacgcctatttttataggttaatgt catgataataatggtttcttagacgtcaggtggcacttttcg gggaaatgtgcgcggaacccctatttgtttatttttctaaat acattcaaatatgtatccgctcatgagacaataaccctgata aatgcttcaataatattgaaaaaggaagagtatgagtattca acatttccgtgtcgcccttattcccttttttgcggcattttg ccttcctgtttttgctcacccagaaacgctggtgaaagtaaa agatgctgaagatcagttgggtgcacgagtgggttacatcga actggatctcaacagcggtaagatccttgagagttttcgccc cgaagaacgttttccaatgatgagcacttttaaagttctgct atgtggcgcggtattatcccgtattgacgccgggcaagagca actcggtcgccgcatacactattctcagaatgacttggttga gtactcaccagtcacagaaaagcatcttacggatggcatgac agtaagagaattatgcagtgctgccataaccatgagtgataa cactgcggccaacttacttctgacaacgatcggaggaccgaa ggagctaaccgcttttttgcacaacatgggggatcatgtaac tcgccttgatcgttgggaaccggagctgaatgaagccatacc aaacgacgagcgtgacaccacgatgcctgtagcaatggcaac aacgttgcgcaaactattaactggcgaactacttactctagc ttcccggcaacaattaatagactggatggaggcggataaagt tgcaggaccacttctgcgctcggcccttccggctggctggtt tattgctgataaatctggagccggtgagcgtgggtctcgcgg tatcattgcagcactggggccagatggtaagccctcccgtat cgtagttatctacacgacggggagtcaggcaactatggatga acgaaatagacagatcgctgagataggtgcctcactgattaa gcattggtaactgtcagaccaagtttactcatatatacttta gattgatttaaaacttcatttttaatttaaaaggatctaggt gaagatcctttttgataatctcatgaccaaaatcccttaacg tgagttttcgttccactgagcgtcagaccccgtagaaaagat caaaggatcttcttgaaatcctttttttctgcgcgtaatctg ctgcttgcaaacaaaaaaaccaccgctaccagcggtggtttg tttgccggatcaagagctaccaactctttttccgaaggtaac tggcttcagcagagcgcagataccaaatactgttcttctagt gtagccgtagttaggccaccacttcaagaactctgtagcacc gcctacatacctcgctctgctaatcctgttaccagtggctgc tgccagtggcgataagtcgtgtcttaccgggttggactcaag acgatagttaccggataaggcgcagcggtcgggctgaacggg gggttcgtgcacacagcccagcttggagcgaacgacctacac cgaactgagatacctacagcgtgagctatgagaaagcgccac gcttcccgaagggagaaaggcggacaggtatccggtaagcgg cagggtcggaacaggagagcgcacgagggagcttccaggggg aaacgcctggtatctttatagtcctgtcgggtttcgccacct ctgacttgagcgtcgatttttgtgatgctcgtcaggggggcg gagcctatggaaaaacgccagcaacgcggcctttttacggtt cctggccttttgctggccttttgctcacatgtcctgcaggcag GENE CASSETTE 59 AG004 OCCURS AT ctgcgcgctcgctcgctcactgaggccgcccgggcgtcgggc BP 1 THROUGH gacctttggtcgcccggcctcagtgagcgagcgagcgcgcag 4438 OF SEQ ID agagggagtggccaactccatcactaggggttcctgcggccg NO: 34 cacgcgttacgtaatatttattgaagtttaatattgtgtttg tgatacagaagtatttgctttaattctaaataaaaattttat gcttttattgctggtttaagaagatttggattatccttgtac tttgaggagaagtttcttatttgaaatattttggaaacaggt cttttaatgtggaaagatagatattaatctcctcttctatta ctctccaagatccaacaaaagtgattataccccccaaaatat gatggtagtatcttatactaccatcattttataggcataggg ctcttagctgcaaataatggaactaactctaataaagcagaa cgcaaatattgtaaatattagagagctaacaatctctgggat ggctaaaggatggagcttggaggctacccagccagtaacaat attccgggctccactgttgaatggagacactacaactgcctt ggatgggcagagatattatggatgctaagccccaggtgctac cattaggacttctaccactgtccctaacgggtggagcccatc acatgcctatgccctcactgtaaggaaatgaagctactgttg tatatcttgggaagcacttggattaattgttatacagttttg ttgaagaagacccctagggtaagtagccataactgcacacta aatttaaaattgttaatgagtttctcaaaaaaaatgttaagg ttgttagctggtatagtatatatcttgcctgttttccaagga cttctttgggcagtaccttgtctgtgctggcaagcaactgag acttaatgaaagagtattggagatatgaatgaattgatgctg tatactctcagagtgccaaacatataccaatggacaagaagg tgaggcagagagcagacaggcattagtgacaagcaaagatat gcagaatttcattctcagcaaatcaaaagtcctcaacctggt tggaagaatattggcactgaatggtatcaataaggttgctag agagggttagaggtgcacaatgtgcttccataacattttata cttctccaatcttagcactaatcaaacatggttgaatacttt gtttactataactcttacagagttataagatctgtgaagaca gggacagggacaatacccatctctgtctggttcataggtggt atgtaatagatatttttaaaaataagtgagttaatgaatgag ggtgagaatgaaggcacagaggtattagggggaggtgggccc cagagaatggtgccaaggtccagtggggtgactgggatcagc tcaggcctgacgctggccactcccacctagctcctttctttc taatctgttctcattctccttgggaaggattgaggtctctgg aaaacagccaaacaactgttatgggaacagcaagcccaaata aagccaagcatcagggggatctgagagctgaaagcaacttct gttccccctccctcagctgaaggggtggggaagggctcccaa agccataactccttttaagggatttagaaggcataaaaaggc ccctggctgagaacttccttcttcattctgcagttggtgaat tccccggggatcctctagagtcgaaattcgccaccatggtga gcaagggcgaggagctgttcaccggggtggtgcccatcctgg tcgagctggacggcgacgtaaacggccacaagttcagcgtgt ccggcgagggcgagggcgatgccacctacggcaagctgaccc tgaagttcatctgcaccaccggcaagctgcccgtgccctggc ccaccctcgtgaccaccctgacctacggcgtgcagtgcttca gccgctaccccgaccacatgaagcagcacgacttcttcaagt ccgccatgcccgaaggctacgtccaggagcgcaccatcttct tcaaggacgacggcaactacaagacccgcgccgaggtgaagt tcgagggcgacaccctggtgaaccgcatcgagctgaagggca tcgacttcaaggaggacggcaacatcctggggcacaagctgg agtacaactacaacagccacaacgtctatatcatggccgaca agcagaagaacggcatcaaggtgaacttcaagatccgccaca acatcgaggacggcagcgtgcagctcgccgaccactaccagc agaacacccccatcggcgacggccccgtgctgctgcccgaca accactacctgagcacccagtccgccctgagcaaagacccca acgagaagcgcgatcacatggtcctgctggagttcgtgaccg ccgccgggatcactctcggcatggacgagctgtacaagtaat agggtaccggtcgacctgcagaagcttgcctcgagcagcgct gctcgagagatctggatcataatcagccataccacatttgta gaggttttacttgctttaaaaaacctcccacacctccccctg aacctgaaacataaaatgaatgcaattgttgttgttaacttg tttattgcagcttataatggttacaaataaagcaatagcatc acaaatttcacaaataaagcatttttttcactgcattctagt tgtggtttgtccaaactcatcaatgtatcttatcatgtctgg taaccattctccaggttgagccagaccaatttgatggtagat ttagcaaataaaaatacaggacacccagttaaatgtgaattt ccgatgaacagcaaatacttttttagtattaaaaaagttcac atttaggctcacgcctgtaatcccagcactttgggaggccga ggcaggcagatcacctgaggtcaggagttcgagaccagcctg gccaacatggtgaaaccccatctccactaaaaataccaaaaa ttagccaggcgtgctggtgggcacctgtagttccagctactc aggaggctaaggcaggagaattgcttgaacctgggaggcaga ggttgcagtgagctgagatcgcaccattgcactctagcctgg gcgacaagaacaaaactccatctcaaaaaaaaaaaaaaaaaa aaagttcacatttaactgggcattctgtatttaattggtaat ctgagatggcagggaacagcatcagcatggtgtgagggatag gcattttttcattgtgtacagcttgtaaatcagtatttttaa aactcaaagttaatggcttgggcatatttagaaaagagttgc cgcacggacttgaaccctgtattcctaaaatctaggatcttg ttctgatggtctgcacaactggctgggggtgtccagccactg tccctcttgcctgggctccccagggcagttctgtcagcctct ccatttccattcctgttccagcaaaacccaactgatagcaca gcagcatttcagcctgtctacctctgtgcccacatacctgga tgtctaccagccagaaaggtggcttagatttggttcctgtgg gtggattatggcccccagaacttccctgtgcttgctgggggt gtggagtggaaagagcaggaaatgggggaccctccgatactc tatgggggtcctccaagtctctttgtgcaagttagggtaata atcaatatggagctaagaaagagaaggggaactatgctttag aacaggacactgtgccaggagcattgcagaaattatatggtt ttcacgacagttctttttggtaggtactgttattatcctcag tttgcagatgaggaaactgagacccagaaaggttaaataact tgctagggtcacacaagtcataactgacaaagcctgattcaa acccaggtctccctaacctttaaggtttctatgacgccagct ctcctagggagtttgtcttcagatgtcttggctctaggtgtc aaaaaaagacttggtgtcaggcaggcataggttcaagtccca actctgtcacttaccaactgtgactaggtgattgaactgacc atggaacctggtcacatgcaggagcaggatggtgaagggttc ttgaaggcacttaggcaggacatttaggcaggagagaaaacc tggaaacagaagagctgtctccaaaaatacccactggggaag caggttgtcatgtgggccatgaatgggacctgttctggggta accacgtgcggaccgagcggccgcaggaacccctagtgatgg agttggccactccctctctgcgcgctcgctcgctcactgagg ccgggcgaccaaaggtcgcccgacgcccgggctttgcccggg cggcctcagtgagcgagcgagcgcgcag Plasmid AG006 Composition 5′ ITR  2 occurs @ bp 1 through bp 119 of SEQ ID NO: 35 Human VMD2 12 Promoter occurs @ bp 134 through bp 761 of SEQ ID NO: 35 Added Kozak  5 occurs @ bp 795 through 800 of SEQ ID NO: 34 E-GFP 24 occurs @ bp 801 through bp 1520 of SEQ ID NO: 35 SV40 POLYA  8 occurs at bp 1578 through bp 1813 of SEQ ID NO: 35 RLBP1 INTRONIC 14 SEQUENCE AS occurs at bp 1821 through bp 3323 of SEQ STUFFER ID NO: 35 SEQUENCE 3′ ITR  9 occurs at bp 3352 through bp 3481 of SEQ ID NO: 35 AMP BACTERIAL 15 BACKBONE occurs at bp 3482 through bp 6100 of SEQ ID NO: 35 Sequence of 35 plasmid AG006 ctgcgcgctcgctcgctcactgaggccgcccgggcgtcgggc gacctttggtcgcccggcctcagtgagcgagcgagcgcgcag agagggagtggccaactccatcactaggggttcctgcggccg cacgcgttacgtaattctgtcattttactagggtgatgaaat tcccaagcaacaccatccttttcagataagggcactgaggct gagagaggagctgaaacctacccggcgtcaccacacacaggt ggcaaggctgggaccagaaaccaggactgttgactgcagccc ggtattcattctttccatagcccacagggctgtcaaagaccc cagggcctagtcagaggctcctccttcctggagagttcctgg cacagaagttgaagctcagcacagccccctaacccccaactc tctctgcaaggcctcaggggtcagaacactggtggagcagat cctttagcctctggattttagggccatggtagagggggtgtt gccctaaattccagccctggtctcagcccaacaccctccaag aagaaattagaggggccatggccaggctgtgctagccgttgc ttctgagcagattacaagaagggactaagacaaggactcctt tgtggaggtcctggcttagggagtcaagtgacggcggctcag cactcacgtgggcagtgccagcctctaagagtgggcaggggc actggccacagagtcccagggagtcccaccagcctagtcgcc agaccgaattccccggggatcctctagagtcgaaattcgcca ccatggtgagcaagggcgaggagctgttcaccggggtggtgc ccatcctggtcgagctggacggcgacgtaaacggccacaagt tcagcgtgtccggcgagggcgagggcgatgccacctacggca agctgaccctgaagttcatctgcaccaccggcaagctgcccg tgccctggcccaccctcgtgaccaccctgacctacggcgtgc agtgcttcagccgctaccccgaccacatgaagcagcacgact tcttcaagtccgccatgcccgaaggctacgtccaggagcgca ccatcttcttcaaggacgacggcaactacaagacccgcgccg aggtgaagttcgagggcgacaccctggtgaaccgcatcgagc tgaagggcatcgacttcaaggaggacggcaacatcctggggc acaagctggagtacaactacaacagccacaacgtctatatca tggccgacaagcagaagaacggcatcaaggtgaacttcaaga tccgccacaacatcgaggacggcagcgtgcagctcgccgacc actaccagcagaacacccccatcggcgacggccccgtgctgc tgcccgacaaccactacctgagcacccagtccgccctgagca aagaccccaacgagaagcgcgatcacatggtcctgctggagt tcgtgaccgccgccgggatcactctcggcatggacgagctgt acaagtaatagggtaccggtcgacctgcagaagcttgcctcg agcagcgctgctcgagagatctggatcataatcagccatacc acatttgtagaggttttacttgctttaaaaaacctcccacac ctccccctgaacctgaaacataaaatgaatgcaattgttgtt gttaacttgtttattgcagcttataatggttacaaataaagc aatagcatcacaaatttcacaaataaagcatttttttcactg cattctagttgtggtttgtccaaactcatcaatgtatcttat catgtctggtaaccattctccaggttgagccagaccaatttg atggtagatttagcaaataaaaatacaggacacccagttaaa tgtgaatttccgatgaacagcaaatacttttttagtattaaa aaagttcacatttaggctcacgcctgtaatcccagcactttg ggaggccgaggcaggcagatcacctgaggtcaggagttcgag accagcctggccaacatggtgaaaccccatctccactaaaaa taccaaaaattagccaggcgtgctggtgggcacctgtagttc cagctactcaggaggctaaggcaggagaattgcttgaacctg ggaggcagaggttgcagtgagctgagatcgcaccattgcact ctagcctgggcgacaagaacaaaactccatctcaaaaaaaaa aaaaaaaaaaaagttcacatttaactgggcattctgtattta attggtaatctgagatggcagggaacagcatcagcatggtgt gagggataggcattttttcattgtgtacagcttgtaaatcag tatttttaaaactcaaagttaatggcttgggcatatttagaa aagagttgccgcacggacttgaaccctgtattcctaaaatct aggatcttgttctgatggtctgcacaactggctgggggtgtc cagccactgtccctcttgcctgggctccccagggcagttctg tcagcctctccatttccattcctgttccagcaaaacccaact gatagcacagcagcatttcagcctgtctacctctgtgcccac atacctggatgtctaccagccagaaaggtggcttagatttgg ttcctgtgggtggattatggcccccagaacttccctgtgctt gctgggggtgtggagtggaaagagcaggaaatgggggaccct ccgatactctatgggggtcctccaagtctctttgtgcaagtt agggtaataatcaatatggagctaagaaagagaaggggaact atgctttagaacaggacactgtgccaggagcattgcagaaat tatatggttttcacgacagttctttttggtaggtactgttat tatcctcagtttgcagatgaggaaactgagacccagaaaggt taaataacttgctagggtcacacaagtcataactgacaaagc ctgattcaaacccaggtctccctaacctttaaggtttctatg acgccagctctcctagggagtttgtcttcagatgtcttggct ctaggtgtcaaaaaaagacttggtgtcaggcaggcataggtt caagtcccaactctgtcacttaccaactgtgactaggtgatt gaactgaccatggaacctggtcacatgcaggagcaggatggt gaagggttcttgaaggcacttaggcaggacatttaggcagga gagaaaacctggaaacagaagagctgtctccaaaaataccca ctggggaagcaggttgtcatgtgggccatgaatgggacctgt tctggggtaaccacgtgcggaccgagcggccgcaggaacccc tagtgatggagttggccactccctctctgcgcgctcgctcgc tcactgaggccgggcgaccaaaggtcgcccgacgcccgggct ttgcccgggcggcctcagtgagcgagcgagcgcgcagctgcc tgcaggggcgcctgatgcggtattttctccttacgcatctgt gcggtatttcacaccgcatacgtcaaagcaaccatagtacgc gccctgtagcggcgcattaagcgcggcgggtgtggtggttac gcgcagcgtgaccgctacacttgccagcgccttagcgcccgc tcctttcgctttcttcccttcctttctcgccacgttcgccgg ctttccccgtcaagctctaaatcgggggctccctttagggtt ccgatttagtgctttacggcacctcgaccccaaaaaacttga tttgggtgatggttcacgtagtgggccatcgccctgatagac ggtttttcgccctttgacgttggagtccacgttctttaatag tggactcttgttccaaactggaacaacactcaactctatctc gggctattcttttgatttataagggattttgccgatttcggt ctattggttaaaaaatgagctgatttaacaaaaatttaacgc gaattttaacaaaatattaacgtttacaattttatggtgcac tctcagtacaatctgctctgatgccgcatagttaagccagcc ccgacacccgccaacacccgctgacgcgccctgacgggcttg tctgctcccggcatccgcttacagacaagctgtgaccgtctc cgggagctgcatgtgtcagaggttttcaccgtcatcaccgaa acgcgcgagacgaaagggcctcgtgatacgcctatttttata ggttaatgtcatgataataatggtttcttagacgtcaggtgg cacttttcggggaaatgtgcgcggaacccctatttgtttatt tttctaaatacattcaaatatgtatccgctcatgagacaata accctgataaatgcttcaataatattgaaaaaggaagagtat gagtattcaacatttccgtgtcgcccttattcccttttttgc ggcattttgccttcctgtttttgctcacccagaaacgctggt gaaagtaaaagatgctgaagatcagttgggtgcacgagtggg ttacatcgaactggatctcaacagcggtaagatccttgagag ttttcgccccgaagaacgttttccaatgatgagcacttttaa agttctgctatgtggcgcggtattatcccgtattgacgccgg gcaagagcaactcggtcgccgcatacactattctcagaatga cttggttgagtactcaccagtcacagaaaagcatcttacgga tggcatgacagtaagagaattatgcagtgctgccataaccat gagtgataacactgcggccaacttacttctgacaacgatcgg aggaccgaaggagctaaccgcttttttgcacaacatggggga tcatgtaactcgccttgatcgttgggaaccggagctgaatga agccataccaaacgacgagcgtgacaccacgatgcctgtagc aatggcaacaacgttgcgcaaactattaactggcgaactact tactctagcttcccggcaacaattaatagactggatggaggc ggataaagttgcaggaccacttctgcgctcggcccttccggc tggctggtttattgctgataaatctggagccggtgagcgtgg gtctcgcggtatcattgcagcactggggccagatggtaagcc ctcccgtatcgtagttatctacacgacggggagtcaggcaac tatggatgaacgaaatagacagatcgctgagataggtgcctc actgattaagcattggtaactgtcagaccaagtttactcata tatactttagattgatttaaaacttcatttttaatttaaaag gatctaggtgaagatcctttttgataatctcatgaccaaaat cccttaacgtgagttttcgttccactgagcgtcagaccccgt agaaaagatcaaaggatcttcttgaaatcctttttttctgcg cgtaatctgctgcttgcaaacaaaaaaaccaccgctaccagc ggtggtttgtttgccggatcaagagctaccaactctttttcc gaaggtaactggcttcagcagagcgcagataccaaatactgt tcttctagtgtagccgtagttaggccaccacttcaagaactc tgtagcaccgcctacatacctcgctctgctaatcctgttacc agtggctgctgccagtggcgataagtcgtgtcttaccgggtt ggactcaagacgatagttaccggataaggcgcagcggtcggg ctgaacggggggttcgtgcacacagcccagcttggagcgaac gacctacaccgaactgagatacctacagcgtgagctatgaga aagcgccacgcttcccgaagggagaaaggcggacaggtatcc ggtaagcggcagggtcggaacaggagagcgcacgagggagct tccagggggaaacgcctggtatctttatagtcctgtcgggtt tcgccacctctgacttgagcgtcgatttttgtgatgctcgtc aggggggcggagcctatggaaaaacgccagcaacgcggcctt tttacggttcctggccttttgctggccttttgctcacatgtc ctgcaggcag GENE CASSETTE 60 OF PLASMID ctgcgcgctcgctcgctcactgaggccgcccgggcgtcgggc AG006 OCCURS AT gacctttggtcgcccggcctcagtgagcgagcgagcgcgcag BP 1 THROUGH agagggagtggccaactccatcactaggggttcctgcggccg 3481 OF SEQ ID cacgcgttacgtaattctgtcattttactagggtgatgaaat NO: 35 tcccaagcaacaccatccttttcagataagggcactgaggct gagagaggagctgaaacctacccggcgtcaccacacacaggt ggcaaggctgggaccagaaaccaggactgttgactgcagccc ggtattcattctttccatagcccacagggctgtcaaagaccc cagggcctagtcagaggctcctccttcctggagagttcctgg cacagaagttgaagctcagcacagccccctaacccccaactc tctctgcaaggcctcaggggtcagaacactggtggagcagat cctttagcctctggattttagggccatggtagagggggtgtt gccctaaattccagccctggtctcagcccaacaccctccaag aagaaattagaggggccatggccaggctgtgctagccgttgc ttctgagcagattacaagaagggactaagacaaggactcctt tgtggaggtcctggcttagggagtcaagtgacggcggctcag cactcacgtgggcagtgccagcctctaagagtgggcaggggc actggccacagagtcccagggagtcccaccagcctagtcgcc agaccgaattccccggggatcctctagagtcgaaattcgcca ccatggtgagcaagggcgaggagctgttcaccggggtggtgc ccatcctggtcgagctggacggcgacgtaaacggccacaagt tcagcgtgtccggcgagggcgagggcgatgccacctacggca agctgaccctgaagttcatctgcaccaccggcaagctgcccg tgccctggcccaccctcgtgaccaccctgacctacggcgtgc agtgcttcagccgctaccccgaccacatgaagcagcacgact tcttcaagtccgccatgcccgaaggctacgtccaggagcgca ccatcttcttcaaggacgacggcaactacaagacccgcgccg aggtgaagttcgagggcgacaccctggtgaaccgcatcgagc tgaagggcatcgacttcaaggaggacggcaacatcctggggc acaagctggagtacaactacaacagccacaacgtctatatca tggccgacaagcagaagaacggcatcaaggtgaacttcaaga tccgccacaacatcgaggacggcagcgtgcagctcgccgacc actaccagcagaacacccccatcggcgacggccccgtgctgc tgcccgacaaccactacctgagcacccagtccgccctgagca aagaccccaacgagaagcgcgatcacatggtcctgctggagt tcgtgaccgccgccgggatcactctcggcatggacgagctgt acaagtaatagggtaccggtcgacctgcagaagcttgcctcg agcagcgctgctcgagagatctggatcataatcagccatacc acatttgtagaggttttacttgctttaaaaaacctcccacac ctccccctgaacctgaaacataaaatgaatgcaattgttgtt gttaacttgtttattgcagcttataatggttacaaataaagc aatagcatcacaaatttcacaaataaagcatttttttcactg cattctagttgtggtttgtccaaactcatcaatgtatcttat catgtctggtaaccattctccaggttgagccagaccaatttg atggtagatttagcaaataaaaatacaggacacccagttaaa tgtgaatttccgatgaacagcaaatacttttttagtattaaa aaagttcacatttaggctcacgcctgtaatcccagcactttg ggaggccgaggcaggcagatcacctgaggtcaggagttcgag accagcctggccaacatggtgaaaccccatctccactaaaaa taccaaaaattagccaggcgtgctggtgggcacctgtagttc cagctactcaggaggctaaggcaggagaattgcttgaacctg ggaggcagaggttgcagtgagctgagatcgcaccattgcact ctagcctgggcgacaagaacaaaactccatctcaaaaaaaaa aaaaaaaaaaaagttcacatttaactgggcattctgtattta attggtaatctgagatggcagggaacagcatcagcatggtgt gagggataggcattttttcattgtgtacagcttgtaaatcag tatttttaaaactcaaagttaatggcttgggcatatttagaa aagagttgccgcacggacttgaaccctgtattcctaaaatct aggatcttgttctgatggtctgcacaactggctgggggtgtc cagccactgtccctcttgcctgggctccccagggcagttctg tcagcctctccatttccattcctgttccagcaaaacccaact gatagcacagcagcatttcagcctgtctacctctgtgcccac atacctggatgtctaccagccagaaaggtggcttagatttgg ttcctgtgggtggattatggcccccagaacttccctgtgctt gctgggggtgtggagtggaaagagcaggaaatgggggaccct ccgatactctatgggggtcctccaagtctctttgtgcaagtt agggtaataatcaatatggagctaagaaagagaaggggaact atgctttagaacaggacactgtgccaggagcattgcagaaat tatatggttttcacgacagttctttttggtaggtactgttat tatcctcagtttgcagatgaggaaactgagacccagaaaggt taaataacttgctagggtcacacaagtcataactgacaaagc ctgattcaaacccaggtctccctaacctttaaggtttctatg acgccagctctcctagggagtttgtcttcagatgtcttggct ctaggtgtcaaaaaaagacttggtgtcaggcaggcataggtt caagtcccaactctgtcacttaccaactgtgactaggtgatt gaactgaccatggaacctggtcacatgcaggagcaggatggt gaagggttcttgaaggcacttaggcaggacatttaggcagga gagaaaacctggaaacagaagagctgtctccaaaaataccca ctggggaagcaggttgtcatgtgggccatgaatgggacctgt tctggggtaaccacgtgcggaccgagcggccgcaggaacccc tagtgatggagttggccactccctctctgcgcgctcgctcgc tcactgaggccgggcgaccaaaggtcgcccgacgcccgggct ttgcccgggcggcctcagtgagcgagcgagcgcgcag Plasmid TM042 Composition ΔITR  1 occurs at bp 4 through bp 106 of SEQ ID NO: 50 Human RLBP1  3 Promoter(short) Occurs at bp 119 through bp 708 of SEQ ID NO: 50 MODIFIED  4 SV40INTRON occurs at bp 723 through bp 905 of SEQ ID NO: 50 Added Kozak  5 occurs at bp 919 through bp 924 of SEQ ID NO: 50 HUMAN RLBP1  6 GENE CDS occurs at bp 925 through bp 1878 of SEQ ID NO: 50 SV40 POLYA  8 occurs at bp 1937 through bp 2172 of SEQ ID NO: 50 3′ ITR  9 occurs at bp 2201 through bp 2330 of SEQ ID NO: 50 KAN-R BACTERIAL 49 BACKBONE occurs at bp 2331 through bp 4989 of SEQ ID NO: 50 Sequence of 50 plasmid TM042 ctgcgcgctcgctcgctcactgaggccgcccgggcaaagccc gggcgtcgggcgacctttggtcgcccggcctcagtgagcgag cgagcgcgcagagagggagtggggtaccacgcgtttgtcctc tccctgcttggccttaaccagccacatttctcaactgacccc actcactgcagaggtgaaaactaccatgccaggtcctgctgg ctgggggaggggtgggcaataggcctggatttgccagagctg ccactgtagatgtagtcatatttacgatttcccttcacctct tattaccctggtggtggtggtgggggggggggggtgctctct cagcaaccccaccccgggatcttgaggagaaagagggcagag aaaagagggaatgggactggcccagatcccagccccacagcc gggcttccacatggccgagcaggaactccagagcaggagcac acaaaggagggctttgatgcgcctccagccaggcccaggcct ctcccctctcccctttctctctgggtcttcctttgccccact gagggcctcctgtgagcccgatttaacggaaactgtgggcgg tgagaagttccttatgacacactaatcccaacctgctgaccg gaccacgcctccagcggagggaacctctagagctccaggaca ttcaggtaccaggtagccccaaggaggagctgccgaatcgat ggatcgggaactgaaaaaccagaaagttaactggtaagttta gtctttttgtcttttatttcaggtcccggatccggtggtggt gcaaatcaaagaactgctcctcagtggatgttgcctttactt ctaggcctgtacggaagtgttacttctgctctaaaagctgcg gaattgtacccgccccgggatccatcgattgaattcgccacc atgtcagaaggggtgggcacgttccgcatggtacctgaagag gaacaggagctccgtgcccaactggagcagctcacaaccaag gaccatggacctgtctttggcccgtgcagccagctgccccgc cacaccttgcagaaggccaaggatgagctgaacgagagagag gagacccgggaggaggcagtgcgagagctgcaggagatggtg caggcgcaggcggcctcgggggaggagctggcggtggccgtg gcggagagggtgcaagagaaggacagcggcttcttcctgcgc ttcatccgcgcacggaagttcaacgtgggccgtgcctatgag ctgctcagaggctatgtgaatttccggctgcagtaccctgag ctctttgacagcctgtccccagaggctgtccgctgcaccatt gaagctggctaccctggtgtcctctctagtcgggacaagtat ggccgagtggtcatgctcttcaacattgagaactggcaaagt caagaaatcacctttgatgagatcttgcaggcatattgcttc atcctggagaagctgctggagaatgaggaaactcaaatcaat ggcttctgcatcattgagaacttcaagggctttaccatgcag caggctgctagtctccggacttcagatctcaggaagatggtg gacatgctccaggattccttcccagcccggttcaaagccatc cacttcatccaccagccatggtacttcaccacgacctacaat gtggtcaagcccttcttgaagagcaagctgcttgagagggtc tttgtccacggggatgacctttctggtttctaccaggagatc gatgagaacatcctgccctctgacttcgggggcacgctgccc aagtatgatggcaaggccgttgctgagcagctctttggcccc caggcccaagctgagaacacagccttctgaggatcgtaccgg tcgacctgcagaagcttgcctcgagcagcgctgctcgagaga tctggatcataatcagccataccacatttgtagaggttttac ttgctttaaaaaacctcccacacctccccctgaacctgaaac ataaaatgaatgcaattgttgttgttaacttgtttattgcag cttataatggttacaaataaagcaatagcatcacaaatttca caaataaagcatttttttcactgcattctagttgtggtttgt ccaaactcatcaatgtatcttatcatgtctggtaaccacgtg cggaccgagcggccgcaggaacccctagtgatggagttggcc actccctctctgcgcgctcgctcgctcactgaggccgggcga ccaaaggtcgcccgacgcccgggctttgcccgggcggcctca gtgagcgagcgagcgcgcagctgcctgcagggttccatccca atggcgcgtcaattcactggccgtcgttttacaacgtcgtga ctgggaaaaccctggcgttacccaacttaatcgccttgcagc acatccccctttcgccagctggcgtaatagcgaagaggcccg caccgatcgcccttcccaacagttgcgcagcctgaatggcga atggcgcctgatgcggtattttctccttacgcatctgtgcgg tatttcacaccgcatatggtgcactctcagtacaatctgctc tgatgccgcatagttaagccagccccgacacccgccaacacc cgctgacgcgccctgacgggcttgtctgctcccggcatccgc ttacagacaagctgtgaccgtctccgggagctgcatgtgtca gaggttttcaccgtcatcaccgaaacgcgcgagacgaaaggg cctcgtgatacgcctatttttataggttaatgtcatgataat aatggtttcttagacgtcaggtggcacttttcggggaaatgt gcgcggaacccctatttgtttatttttctaaatacattcaaa tatgtatccgctcatgagacaataaccctgataaatgcttca ataatattgaaaaaggaagagtatgagccatattcaacggga aacgtcttgctctaggccgcgattaaattccaacatggatgc tgatttatatgggtataaatgggctcgcgataatgtcgggca atcaggtgcgacaatctatcgattgtatgggaagcccgatgc gccagagttgtttctgaaacatggcaaaggtagcgttgccaa tgatgttacagatgagatggtcagactaaactggctgacgga atttatgcctcttccgaccatcaagcattttatccgtactcc tgatgatgcatggttactcaccactgcgatccctgggaaaac agcattccaggtattagaagaatatcctgattcaggtgaaaa tattgttgatgcgctggcagtgttcctgcgccggttgcattc gattcctgtttgtaattgtccttttaacagcgatcgcgtatt tcgtctcgctcaggcgcaatcacgaatgaataacggtttggt tgatgcgagtgattttgatgacgagcgtaatggctggcctgt tgaacaagtctggaaagaaatgcataaacttttgccattctc accggattcagtcgtcactcatggtgatttctcacttgataa ccttatttttgacgaggggaaattaataggttgtattgatgt tggacgagtcggaatcgcagaccgataccaggatcttgccat cctatggaactgcctcggtgagttttctccttcattacagaa acggctttttcaaaaatatggtattgataatcctgatatgaa taaattgcagtttcatttgatgctcgatgagtttttctaact gtcagaccaagtttactcatatatactttagattgatttaaa acttcatttttaatttaaaaggatctaggtgaagatcctttt tgataatctcatgaccaaaatcccttaacgtgagttttcgtt ccactgagcgtcagaccccgtagaaaagatcaaaggatcttc ttgagatcctttttttctgcgcgtaatctgctgcttgcaaac aaaaaaaccaccgctaccagcggtggtttgtttgccggatca agagctaccaactctttttccgaaggtaactggcttcagcag agcgcagataccaaatactgttcttctagtgtagccgtagtt aggccaccacttcaagaactctgtagcaccgcctacatacct cgctctgctaatcctgttaccagtggctgctgccagtggcga taagtcgtgtcttaccgggttggactcaagacgatagttacc ggataaggcgcagcggtcgggctgaacggggggttcgtgcac acagcccagcttggagcgaacgacctacaccgaactgagata cctacagcgtgagctatgagaaagcgccacgcttcccgaagg gagaaaggcggacaggtatccggtaagcggcagggtcggaac aggagagcgcacgagggagcttccagggggaaacgcctggta tctttatagtcctgtcgggtttcgccacctctgacttgagcg tcgatttttgtgatgctcgtcaggggggcggagcctatggaa aaacgccagcaacgcggcctttttacggttcctggccttttg ctggccttttgctcacatgttctttcctgcgttatcccctga ttctgtggataaccgtattaccgcctttgagtgagctgatac cgctcgccgcagccgaacgaccgagcgcagcgagtcagtgag cgaggaagcggaagagcgcccaatacgcaaaccgcctctccc cgcgcgttggccgattcattaatgcagctggcacgacaggtt tcccgactggaaagcgggcagtgagcgcaacgcaattaatgt gagttagctcactcattaggcaccccaggctttacactttat gcttccggctcgtatgttgtgtggaattgtgagcggataaca atttcacacaggaaacagctatgaccatgattacgccaagct cggcgcgccattgggatggaaccctgcaggcag GENE CASSETTE 61 TM042 OCCURS AT cgcgctcgctcgctcactgaggccgcccgggcaaagcccggg BP 4 THROUGH cgtcgggcgacctttggtcgcccggcctcagtgagcgagcga 2330 OF SEQ ID gcgcgcagagagggagtggggtaccacgcgtttgtcctctcc NO: 50 ctgcttggccttaaccagccacatttctcaactgaccccact cactgcagaggtgaaaactaccatgccaggtcctgctggctg ggggaggggtgggcaataggcctggatttgccagagctgcca ctgtagatgtagtcatatttacgatttcccttcacctcttat taccctggtggtggtggtgggggggggggggtgctctctcag caaccccaccccgggatcttgaggagaaagagggcagagaaa agagggaatgggactggcccagatcccagccccacagccggg cttccacatggccgagcaggaactccagagcaggagcacaca aaggagggctttgatgcgcctccagccaggcccaggcctctc ccctctcccctttctctctgggtcttcctttgccccactgag ggcctcctgtgagcccgatttaacggaaactgtgggcggtga gaagttccttatgacacactaatcccaacctgctgaccggac cacgcctccagcggagggaacctctagagctccaggacattc aggtaccaggtagccccaaggaggagctgccgaatcgatgga tcgggaactgaaaaaccagaaagttaactggtaagtttagtc tttttgtcttttatttcaggtcccggatccggtggtggtgca aatcaaagaactgctcctcagtggatgttgcctttacttcta ggcctgtacggaagtgttacttctgctctaaaagctgcggaa ttgtacccgccccgggatccatcgattgaattcgccaccatg tcagaaggggtgggcacgttccgcatggtacctgaagaggaa caggagctccgtgcccaactggagcagctcacaaccaaggac catggacctgtctttggcccgtgcagccagctgccccgccac accttgcagaaggccaaggatgagctgaacgagagagaggag acccgggaggaggcagtgcgagagctgcaggagatggtgcag gcgcaggcggcctcgggggaggagctggcggtggccgtggcg gagagggtgcaagagaaggacagcggcttcttcctgcgcttc atccgcgcacggaagttcaacgtgggccgtgcctatgagctg ctcagaggctatgtgaatttccggctgcagtaccctgagctc tttgacagcctgtccccagaggctgtccgctgcaccattgaa gctggctaccctggtgtcctctctagtcgggacaagtatggc cgagtggtcatgctcttcaacattgagaactggcaaagtcaa gaaatcacctttgatgagatcttgcaggcatattgcttcatc ctggagaagctgctggagaatgaggaaactcaaatcaatggc ttctgcatcattgagaacttcaagggctttaccatgcagcag gctgctagtctccggacttcagatctcaggaagatggtggac atgctccaggattccttcccagcccggttcaaagccatccac ttcatccaccagccatggtacttcaccacgacctacaatgtg gtcaagcccttcttgaagagcaagctgcttgagagggtcttt gtccacggggatgacctttctggtttctaccaggagatcgat gagaacatcctgccctctgacttcgggggcacgctgcccaag tatgatggcaaggccgttgctgagcagctctttggcccccag gcccaagctgagaacacagccttctgaggatcgtaccggtcg acctgcagaagcttgcctcgagcagcgctgctcgagagatct ggatcataatcagccataccacatttgtagaggttttacttg ctttaaaaaacctcccacacctccccctgaacctgaaacata aaatgaatgcaattgttgttgttaacttgtttattgcagctt ataatggttacaaataaagcaatagcatcacaaatttcacaa ataaagcatttttttcactgcattctagttgtggtttgtcca aactcatcaatgtatcttatcatgtctggtaaccacgtgcgg accgagcggccgcaggaacccctagtgatggagttggccact ccctctctgcgcgctcgctcgctcactgaggccgggcgacca aaggtcgcccgacgcccgggctttgcccgggcggcctcagtg agcgagcgagcgcgcag

TABLE 3 Plasmid Construction SEQUENCE IDENTIFIER (SEQ. ID. NO:) Construction summary Plasmid TM017 1 PvuII/MluI restriction fragment of Δ5′ ITR ΔITR element cloned into PvuII/MluI restriction fragment of plasmid backbone 3 Blunted BamHI/MluI restriction fragment of Human RLBP1 human RLBP1 promoter (short) was cloned Promoter(short) into blunted SacII/MluI restriction fragment of plasmid backbone 4 MluI/ClaI restriction fragment a clone MODIFIED containing an hCMV promoter and modified SV40INTRON SV40 intron was cloned into MluI/ClaI restriction fragment of plasmid backbone. The hCMV promoter was removed during subsequent cloning to insert human RLBP1 promoter (short) 5, 6 EcoRI/AgeI restriction fragment containing Added Kozak Kozak and human RLBP1 gene CDS was cloned AND HUMAN into EcoRI/AgeI restriction fragment of RLBP1 plasmid backbone GENE CDS 8 BglII/BstEII restriction fragment of SV40 SV40 POLYA polyA was cloned into BglII/BsteII restriction fragment of the plasmid backbone 9 Present in original Amp resistant 3′ ITR backbone, AAV-MCS (Stratagene) Plasmid TM037 construction summary 2 Present in original Amp resistant 5′ ITR backbone, AAV-MCS (Stratagene) 10 Blunted HindIII/EcoRI restriction fragment Human RLBP1 of human RLBP1 promoter (long) was cloned Promoter(long) into blunted MluI/EcoRI restriction fragment of plasmid backbone 5, 6 EcoRI/AgeI restriction fragment containing Added Kozak Kozak and human RLBP1 gene CDS cloned into AND HUMAN EcoRI/AgeI restriction fragment of plasmid RLBP1 backbone GENE CDS 8 BglII/BstEII restriction fragment SV40 POLYA containing SV40 polyA was cloned into BglII/BsteII restriction fragment of the plasmid backbone 9 Present in original Amp resistant 3′ ITR backbone, AAV-MCS (Stratagene) Plasmid AG007 construction summary 2 Present in original Amp resistant 5′ ITR backbone, pAAV-MCS (Stratagene) 11 MluI/EcoRI restriction fragment containing Human RPE65 human RPE65 promoter cloned into Promoter MluI/EcoRI restriction fragment of the plasmid backbone 5, 6 EcoRI/AgeI restriction fragment containing ADDED-KOZAK Kozak and human RLBP1 gene CDS cloned into and HUMAN RLBP1 EcoRI/AgeI restriction fragment of plasmid GENE CDS backbone 8 BglII/BstEII restriction fragment SV40 POLYA containing SV40 polyA was cloned into BglII/BsteII restriction fragment of the plasmid backbone 14 BstEII restriction fragment containing RLBP1 INTRONIC RLBP1 intron1 stuffer sequence was cloned SEQUENCE AS into BstEII restriction fragment of the STUFFER plasmid backbone SEQUENCE 9 Present in original Amp resistant 3′ ITR backbone, pAAV-MCS (Stratagene) Plasmid TM039 construction summary 2 Present in original Amp resistant 5′ ITR backbone, AAV-MCS purchased from Stratagene 22 EcoRI/MluI restriction fragment containing CMV-enhancer CMV-enhancer with CBA promoter was cloned with CBA into EcoRI/MluI restriction fragment of promoter plasmid backbone 5, 6 EcoRI/SalI restriction fragment containing Added Kozak Kozak and human RLBP1 gene CDS was cloned AND HUMAN into EcoRI/SalI restriction fragment of RLBP1 plasmid backbone GENE CDS 8 BglII/BstEII restriction fragment SV40 POLYA containing SV40 polyA was cloned into BglII/BsteII restriction fragment of the plasmid backbone 23 REVERSE Plasmid backbone was cut with BstEII then COMPLEMENT OF blunted. The stuffer was PCR amplified RLBP1 INTRON from human cell line (HEK293 or ARPE19) STUFFER genomic DNA, the product was phosphorylated and ligated into backbone. 9 Present in original Amp resistant 3′ ITR backbone, AAV-MCS (Stratagene) Plasmid TM040 construction summary 2 Present in original Amp resistant 5′ ITR backbone, AAV-MCS (Stratagene) 3 Blunted BamHI/MluI restriction fragment of Human RLBP1 human RLBP1 promoter (short) was cloned promoter into blunted SacII/MluI restriction (short) fragment of plasmid backbone 4 MluI/ClaI restriction fragment containing MODIFIED an hCMV promoter and modified SV40 intron SV40INTRON was cloned into MluI/ClaI restriction fragment of plasmid backbone. The hCMV promoter was removed during subsequent cloning to insert human RLBP1 promoter (short) 5, 6 EcoRI/SalI restriction fragment containing Added Kozak Kozak and human RLBP1 gene CDS cloned into AND HUMAN EcoRI/SalI restriction fragment of plasmid RLBP1 backbone GENE CDS 8 BglII/BstEII restriction fragment SV40 POLYA containing SV40 polyA was cloned into BglII/BsteII restriction fragment of the plasmid backbone 23 REVERSE Plasmid backbone was cut with BstEII then COMPLEMENT OF blunted. The stuffer was PCR amplified RLBP1 INTRON from human cell line (HEK293 or ARPE19) STUFFER genomic DNA, the product was phosphorylated and ligated into backbone. 9 Present in original Amp resistant 3′ ITR backbone, AAV-MCS purchased from Stratagene Plasmid TM016 construction summary 1 PvuII/MluI restriction of Δ5′ ITR element Δ5′ ITR cloned into PvuII/MluI restriction fragment of plasmid backbone 3 Blunted BamHI/MluI restriction fragment of Human RLBP1 human RLBP1 promoter (short) was cloned promoter into blunted SacII/MluI restriction (short) fragment of plasmid backbone 4 MluI/ClaI restriction fragment of MODIFIED containing an hCMV promoter and modified SV40INTRON SV40 intron was cloned into MluI/ClaI restriction fragment of plasmid backbone. The hCMV promoter was removed during subsequent cloning to insert human RLBP1 promoter (short) 24 EcoRI/Age fragment containing GFP was E_GFP blunted then cloned into the SalI digested and blunted backbone 8 BglII/BstEII restriction fragment SV40 POLYA containing SV40 polyA was cloned into BglII/BsteII restriction fragment of the plasmid backbone 9 Present in original Amp resistant 3′ ITR backbone, AAV-MCS purchased from Stratagene Plasmid TM035 construction summary 2 Present in original Amp resistant 5′ ITR backbone, AAV-MCS purchased from Stratagene 10 Blunted HindIII/EcoRI restriction fragment Human RLBP1 of human RLBP1 promoter (long) was cloned promoter (long) into blunted MluI/EcoRI restriction fragment of plasmid backbone 24 EcoRI/Age I digested fragment containing E_GFP GFP was blunted then cloned into the SalI digested and blunted backbone 8 BglII/BstEII restriction fragment SV40 POLYA containing SV40 polyA was cloned into BglII/BstEII restriction fragment of the plasmid backbone 9 Present in original Amp resistant 3′ ITR backbone, AAV-MCS purchased from Stratagene Plasmid AG012 construction summary 2 Present in original Amp resistant 5′ ITR backbone, AAV-MCS purchased from Stratagene 13 The plasmid backbone was digested with SYNUCLEIN MluI/AgeI. INTRONIC The synuclein stuffer was PCR amplified SEQUENCE AS from plasmid pBV5, the product was STUFFER digested with MluI/AgeI, phosphorylated SEQUENCE and ligated into the plasmid backbone. 8 BglII/BstEII restriction fragment from SV40 POLYA GeneArt synthesized clone containing SV40 polyA was cloned into BglII/BstEII restriction fragment of the plasmid backbone 14 BstEII restriction fragment from RLBP1 INTRONIC intermediary clone containing RLBP1 SEQUENCE AS intron1 stuffer sequence cloned into STUFFER BstEII restriction fragment of the plasmid SEQUENCE backbone 9 Present in original Amp resistant 3′ ITR backbone, AAV-MCS purchased from Stratagene Plasmid AG004 construction summary 2 Present in original Amp resistant 5′ ITR backbone, AAV-MCS purchased from Stratagene 11 MluI/EcoRI restriction fragment from Human RPE65 GeneArt synthesized clone containing human Promoter RPE65 promoter cloned into MluI/EcoRI restriction fragment of the plasmid backbone 24 An EcoRI/AgeI digested fragment from an E_GFP intermediary clone was blunted then cloned into the SalI digested and blunted backbone 8 BglII/BstEII restriction fragment from SV40 POLYA GeneArt synthesized clone containing SV40 polyA was cloned into BglII/BstEII restriction fragment of the plasmid backbone 14 BstEII restriction fragment from RLBP1 INTRONIC intermediary clone containing RLBP1 SEQUENCE AS intron1 stuffer sequence cloned into STUFFER BstEII restriction fragment of the plasmid SEQUENCE backbone 9 Present in original Amp resistant 3′ ITR backbone, AAV-MCS purchased from Stratagene Plasmid AG006 construction summary 2 Present in original Amp resistant 5′ ITR backbone, AAV-MCS purchased from Stratagene 12 MluI/EcoRI restriction fragment from HUMAN VMD2 GeneArt synthesized clone containing human PROMOTER VMD2 promoter cloned into MluI/EcoRI restriction fragment of the plasmid backbone 24 An EcoRI/AgeI digested fragment from an E_GFP intermediary clone was blunted then cloned into the SalI digested and blunted backbone 8 BglII/BstEII restriction fragment from SV40 POLYA GeneArt synthesized clone containing SV40 polyA was cloned into BglII/BstEII restriction fragment of the plasmid backbone 14 BstEII restriction fragment from RLBP1 INTRONIC intermediary clone containing RLBP1 SEQUENCE AS intron1 stuffer sequence cloned into STUFFER BstEII restriction fragment of the plasmid SEQUENCE backbone 9 Present in original Amp resistant 3′ ITR backbone, AAV-MCS purchased from Stratagene Plasmid TM042 Construction Summary 1-ΔITR, 3- SbfI restriction fragment of Plamsid Human RLBP1 pTM017 was cloned into a SbfI restriction Promoter(short), fragment of Puc57 with kanamycin 4- MODIFIED resistance gene backbone. SV40INTRON, 5, 6- Added Kozak AND HUMAN RLBP1 GENE, 8- SV40 POLYA, and 9- 3′ ITR

TABLE 4 Viral Vector Composition: Vector Genome and Caspid SEQUENCE SEQUENCE IDENTIFIER ELEMENTS (SEQ. ID. NO:) Viral Vector NVS1 (Generated from plasmid TM017 or TM042, and AAVRep2/Cap2 plasmid) The viral vector contains a self complementary genome with the following genomic elements in the 5′ to 3′ direction packaged in the viral capsid AAV2. SC5′ ITR 36 Reverse 62 Complementary sequence of SV40polyA Reverse 63 Complementary sequence of HUMAN RLBP1 GENE CDS Reverse 64 Complementary sequence of Added KOZAK Reverse 65 Complementary sequence of Modified SV40INTRON Reverse 66 Complementary sequence of Human RLBP1 PROMOTER (short) ΔITR 1 Human RLBP1 3 PROMOTER (short) Modified 4 SV40INTRON Added Kozak 5 HUMAN RLBP1 6 GENE CDS SV40 POLYA 8 3′ ITR 9 CAPSID PROTEIN SEQUENCE OF NVS1 AAV2 CAPSID 19, 68 and 69 SEQUENCE (Encoded by 18) Viral Vector NVS2 (Generated from plasmid TM017 or TM042, and AAVRep2/Cap8 plasmid) The viral vector contains a self complementary genome with the following genomic elements in the 5′ to 3′ direction packaged in the viral capsid AAV8. SC5′ ITR 36 Reverse 62 Complementary sequence of SV40polyA Reverse 63 Complementary sequence of HUMAN RLBP1 GENE CDS Reverse 64 Complementary sequence of Added KOZAK Reverse 65 Complementary sequence of Modified SV40INTRON Reverse 66 Complementary sequence of Human RLBP1 PROMOTER (short) ΔITR 1 Human RLBP1 3 PROMOTER (short) Modified 4 SV40INTRON Added Kozak 5 HUMAN RLBP1 6 GENE CDS SV40 POLYA 8 3′ ITR 9 CAPSID PROTEIN SEQUENCE OF NVS2 AAV8 CAPSID 21, 70, and 71 SEQUENCE (Encoded by 20) Viral Vector NVS3 (Generated from plasmid TM037 and AAVRep2/Cap2 plasmid) The viral vector genome contains the following genomic elements in the 5′ to 3′ direction 5′ ITR 2 HUMAN RLBP1 10 PROMOTER (long) ADDED KOZAK 5 HUMAN RLBP1 6 GENE CDS SV40 POLYA 8 3′ ITR 9 CAPSID PROTEIN SEQUENCE OF NVS3 AAV2 CAPSID 19, 68 and 69 SEQUENCE (Encoded by 18) Viral Vector NVS4 (Generated from plasmid TM037 and AAVRep2/Cap8 plasmid) The viral vector genome contains the following genomic elements in the 5′ to 3′ direction 5′ ITR 2 HUMAN RLBP1 10 PROMOTER (long) ADDED KOZAK 5 HUMAN RLBP1 6 GENE CDS SV40 POLYA 8 3′ ITR 9 CAPSID PROTEIN SEQUENCE OF NVS4 AAV8 CAPSID 21, 70, and 71 SEQUENCE (Encoded by 20) Viral Vector NVS5 (Generated from plasmid AG007 and AAVRep2/Cap2 plasmid) The viral vector genome contains the following genomic elements in the 5′ to 3′ direction 5′ ITR 2 HUMAN RPE65 11 PROMOTER ADDED-KOZAK 5 HUMAN RLBP1 6 GENE CDS SV40 POLYA 8 RLBP1 INTRONIC 14 SEQUENCE AS STUFFER SEQUENCE 3′ ITR 9 CAPSID PROTEIN SEQUENCE OF NVS5 AAV2 CAPSID 19, 68 and 69 SEQUENCE (Encoded by 18) Viral Vector NVS6 (Generated from plasmid AG007 and AAVRep2/Cap8 plasmid) The viral vector genome contains the following genomic elements in the 5′ to 3′ direction 5′ ITR 2 HUMAN RPE65 11 PROMOTER ADDED-KOZAK 5 HUMAN RLBP1 6 GENE CDS SV40 POLYA 8 RLBP1 INTRONIC 14 SEQUENCE AS STUFFER SEQUENCE 3′ ITR 9 CAPSID PROTEIN SEQUENCE OF NVS6 AAV8 CAPSID 21, 70, and 71 SEQUENCE (Encoded by 20) Viral Vector NVS7 (Generated from plasmid TM039 and AAVRep2/Cap2 plasmid) The viral vector genome contains the following genomic elements in the 5′ to 3′ direction 5′ ITR 2 CMV Enhancer 22 and CBA PROMOTER (GENEBANK ACCESSION DD215332 FROM BP 1 to BP 161) ADDED KOZAK 5 HUMAN RLBP1 6 GENE CDS SV40 POLYA 8 REVERSE 23 COMPLEMENT OF RLBP1 INTRONIC SEQUENCE AS STUFFER SEQUENCE (NT 010274.17) 3′ ITR 9 CAPSID PROTEIN SEQUENCE OF NVS7 AAV2 CAPSID 19, 68 and 69 SEQUENCE (Encoded by 18) Viral Vector NVS8 (Generated from plasmid TM039 and AAVRep2/Cap8 plasmid) The viral vector genome contains the following genomic elements in the 5′ to 3′ direction 5′ ITR 2 CMV Enhancer 22 and CBA PROMOTER (GENEBANK ACCESSION DD215332 FROM BP 1 to BP 161) ADDED KOZAK 5 HUMAN RLBP1 6 GENE CDS SV40 POLYA 8 REVERSE 23 COMPLEMENT OF RLBP1 INTRONIC SEQUENCE AS STUFFER SEQUENCE (NT 010274.17) 3′ ITR 9 CAPSID PROTEIN SEQUENCE OF NVS8 AAV8 CAPSID 21, 70, and 71 SEQUENCE (Encoded by 20) Viral Vector NVS9 (Generated from plasmid TM040 and AAVRep2/Cap2 plasmid) The viral vector genome contains the following genomic elements in the 5′ to 3′ direction 5′ ITR 2 HUMAN RLBP1 3 PROMOTER (short) MODIFIED SV40 4 INTRON ADDED KOZAK 5 HUMAN RLBP1 6 GENE CDS SV40 POLYA 8 REVERSE 23 COMPLEMENT OF RLBP1 INTRONIC SEQUENCE AS STUFFER SEQUENCE (NT_010274.17) 3′ ITR 9 CAPSID PROTEIN SEQUENCE OF NVS9 AAV2 CAPSID 19, 68 and 69 SEQUENCE (Encoded by 18) Viral Vector NVS10 (Generated from plasmid TM040 and AAVRep2/Cap8 plasmid) The viral vector genome contains the following genomic elements in the 5′ to 3′ direction 5′ ITR 2 HUMAN RLBP1 3 PROMOTER (short) MODIFIED SV40 4 INTRON ADDED KOZAK 5 HUMAN RLBP1 6 GENE CDS SV40 POLYA 8 REVERSE 23 COMPLEMENT OF RLBP1 INTRONIC SEQUENCE AS STUFFER SEQUENCE (NT_010274.17) 3′ ITR 9 CAPSID PROTEIN SEQUENCE OF NVS10 AAV8 CAPSID 21, 70, and 71 SEQUENCE (Encoded by 20) Viral vector scAAV8-pRLBP1(short)-eGFP (eGFP Reporter viral vector generated from plasmid TM016 and AAVRep2/Cap8 plasmid) The viral vector contains a self complementary genome with the following genomic elements in the 5′ to 3′ direction packaged in the viral capsid AAV8. SC5′ ITR 36 Reverse 62 Complementary sequence of SV40polyA Reverse 67 Complementary sequence of eGFP Reverse 64 Complementary sequence of Added KOZAK Reverse 65 Complementary sequence of Modified SV40INTRON Reverse 66 Complementary sequence of Human RLBP1 PROMOTER (short) ΔITR 1 HUMAN RLBP1 3 PROMOTER (short) MODIFIED SV40 4 INTRON ADDED KOZAK 5 eGFP 24 SV40 POLYA 8 3′ ITR 9 CAPSID PROTEIN SEQUENCE OF Viral vector scAAV8- pRLBP1(short)-eGFP AAV8 CAPSID 21, 70, and 71 SEQUENCE (Encoded by 20) Viral Vector AAV8-pRLBP1(long)-eGFP (eGFP Reporter viral vector generated from plasmid TM035 and AAVRep2/Cap8 plasmid) The viral vector genome contains the following genomic elements in the 5′ to 3′ direction 5′ ITR 2 HUMAN RLBP1 10 PROMOTER (long) ADDED KOZAK 5 eGFP 24 SV40 POLYA 8 3′ ITR 9 CAPSID PROTEIN SEQUENCE OF Viral Vector AAV8-pRLBP1(long)-eGFP AAV8 CAPSID 21, 70, and 71 SEQUENCE (Encoded by 20) Viral Vector AAV8-pRPE65-eGFP (eGFP Reporter viral vector generated from plasmid AG004 and AAVRep2/Cap8 plasmid) The viral vector genome contains the following genomic elements in the 5′ to 3′ direction 5′ ITR 2 HUMAN RPE65 11 PROMOTER ADDED KOZAK 5 eGFP 24 SV40 POLYA 8 RLBP1 INTRONIC 14 SEQUENCE AS STUFFER SEQUENCE (NT_010274.17) 3′ ITR 9 CAPSID PROTEIN SEQUENCE OF Viral Vector AAV8-pRPE65-eGFP AAV8 CAPSID 21, 70, and 71 SEQUENCE (Encoded by 20) Viral Vector AAV8-pVMD2-eGFP (eGFP Reporter viral vector generated from plasmid AG006 and AAVRep2/Cap8 plasmid) The viral vector genome contains the following genomic elements in the 5′ to 3′ direction 5′ ITR 2 HUMAN VMD2 12 PROMOTER ADDED KOZAK 5 eGFP 24 SV40 POLYA 8 RLBP1 INTRONIC 14 SEQUENCE AS STUFFER SEQUENCE (NT_010274.17) 3′ ITR 9 CAPSID PROTEIN SEQUENCE OF Viral Vector AAV8-pVMD2-eGFP AAV8 CAPSID 21, 70, and 71 SEQUENCE (Encoded by 20) Viral Vector NVS11 (Generated from plasmid AG012 and AAVRep2/Cap8 plasmid) The viral vector genome contains the following genomic elements in the 5′ to 3′ direction 5′ ITR 2 SYNUCLEIN 13 INTRONIC SEQUENCE AS STUFFER SEQUENCE SV40 POLYA 8 RLBP1 INTRONIC 14 SEQUENCE AS STUFFER SEQUENCE (NT_010274.17) 3′ ITR 9 CAPSID PROTEIN SEQUENCE OF NVS11 AAV8 CAPSID 21, 70, and 71 SEQUENCE (Encoded by 20)

Example 2 Subretinal Injection of rAAV Vectors in Mice

2.1 Subretinal Injection of rAAV Vectors in Mice

Subretinal injection of an rAAV vector can achieve efficient transduction of RPE and other retinal cells because subretinal injection induces a bleb of concentrated virus in intimate contact with RPE cells and the neural retina. In addition, the subretinal space has a relatively high degree of immunoprivilege and typically very little evidence of inflammation is seen in the vicinity of the injection site. Thus, subretinal injection was a preferred route for delivery of rAAV vectors in mouse retina. However, other routes of delivery may be used, for example, intravitreal injection.

Supplies/reagents:

Leica M844 F40 Ophthalmic Surgical Microscope

1% cyclopentolate: Bausch & Lomb Cat#965911

2.5%-10% phenylephrine: Altaire Pharmaceuticals Cat#05626

0.5% Proparacaine: Bausch & Lomb Cat#NDC 54799-500-12

10 μl Hamilton syringe: VWR Cat#89184-476

33G blunt-ended needle: Hamilton Cat#7803-05

Fluorescein sodium salt: Sigma Cat#F6377

Test Articles Used in this Example:

scAAV8-pRLBP1(short)-eGFP viral vector 1×10⁹ vg/eye

AAV8-pRLBP1(long)-eGFP viral vector 1×10⁹ vg/eye

AAV8-pRPE-eGFP viral vector 1×10⁹ vg/eye

AAV8-VMD2-eGFP viral vector 1×10⁹ vg/eye

Protocol:

The subretinal injection was performed either in both eyes or unilaterally in the right eye. All procedures were performed under aseptic conditions, using sterile reagents, syringes and appropriate personal protection equipment.

Subretinal Injection Procedures:

-   -   The mouse pupils were dilated by 1 drop of 1% cyclopentolate and         followed by 1 drop of 2.5%-10% phenylephrine     -   The mouse was anesthetized by using Avertin (250 mg/kg) i.p. and         a drop of 0.5% Proparacine topically (local anesthetic) in the         eye     -   An approximately 0.5 mm incision was made nasally, posterior to         the limbus with a microscalpel     -   The blunt-ended needle on the 10 μl Hamilton syringe was         inserted tangentially through the scleral incision toward the         temporal retina. The needle was advanced until resistance was         felt. The 1 μl of diluted rAAV vector (containing fluorescein         with the concentration of 1:50) was then injected slowly into         the subretinal space, and the needle is withdrawn through the         incision     -   The eye was examined and the success of the subretinal injection         was confirmed by visualization of a bleb containing fluorescein.         The success of injection and the degree of retinal damage         (hemorrhage) were scored.     -   An antibiotic ointment was applied to the eye immediately after         the injection         2.2. rAAV Vectors Induced GFP Expression and its Cell-Type         Specifics in Mouse Retina

To study the rAAV vector-induced gene transduction and cell-type specifics in the mouse retina, the eGFP expression in retinal cross sections and RPE/retina flatmounts were examined. One approach used to identify the eGFP expressing cell types was to co-label eGFP positive cells with retinal cell markers by immunocytochemistry staining in cryosections.

Supplies/Reagents: Primary Antibodies for Immunocytochemistry Staining:

-   -   Anti-CRALBP antibody: Thermo cat#MA1-813     -   Anti-GFAP antibody: Covance cat#SMI-21     -   Anti-Opsin Blue antibody: Millipore cat#AB 5407     -   Anti-Opsin Red antibody: Millipore cat#AB5405     -   Anti-Vimentin antibody: Santa Cruz cat#sc-7557     -   Anti-PKC α antibody: C-20 Santa Cruz cat#sc -208

Secondary Antibodies for Immunocytochemistry Staining:

-   -   Goat anti-mouse IgG: Invitrogen Cat#A11005     -   Goat anti-rat IgG: Invitrogen Cat#A11007     -   Donkey anti-rabbit IgG: Invitrogen Cat#A21207

Other Supplies/Reagents:

-   -   Vectashield Mounting Medium with DAPI: Vector Laboratories,         Burlingame Cat#H-1200),     -   Zeiss Imaging system, AxioVision Software     -   Zeiss LSM 510 confocal microscope, ZEN version of the Zeiss         software Protocol:

The mouse eyeball was removed and placed in 4% PFA (paraformaldehyde) for 2 hours at 25° C. and then in PBS buffer for 1-3 days in 4° C. till dissection. The cornea, lens and vitreous were removed from the eye ball and the retinal and RPE/choroid was flatmounted with Vectashield mounting medium on to the slide. The GFP expression in flatmount was captured by Zeiss Imaging system and quantified using AxioVision Software. After imaging, the slides with retinal flatmounts were placed in 0.25% triton buffer at 25° C. for 30 min and then the retinal flatmounts were removed from the slides. The eGFP positive areas of the retina flatmounts were cut and embedded in OCT and then cryosectioned. The immunocytochemistry staining using retinal cell markers was applied in the cryosections. The images were captured by Zeiss LSM 510 confocal microscope and ZEN version of the Zeiss software.

The Immunocytochemistry Staining Procedures: Day 1.

-   -   air dry sections at room temperature 1 hour.     -   place slides in PBS+0.25% Triton 15 min×2     -   block in 1% BSA+PBS+0.25% Triton 90 min     -   incubate slides with primary antibody in 1% BSA+PBS+0.25% Triton         at 4° C. overnight

Day 2.

-   -   take out slides from 4° C., leave them at 25° C. for 30 min     -   wash slides in PBS+0.25% Triton 15 min×2     -   incubate slides with secondary 1:800 at 25° C. for 90 min     -   wash slides in PBS+0.25% Triton 15 min×2     -   mount slides with Vectashield Mounting Medium with DAPI

TABLE 5 The retinal cell markers and dilutions used in the study Cell Type Cell Marker Dilutions Müller cell Anti-CRALBP  1:1000 Anti-Vimentin 1:100 Anti-GFAP  1:1000 Photoreceptor Anti-Opsin Red/Green 1:250 Anti-Opsin Blue 1:250 Neuron in INL Anti-PKCα 1:200 Astrocytes Anti-GFAP  1:1000

TABLE 6 Immunohistochemistry results that describe the transduction of cell types by test viral vectors. scAAV8- AAV8- AAV8- AAV8 Cell Type Cell Marker pRLBP1(short)-eGFP pRLBP1(long)-eGFP pRPE65-eGFP pVMD2-eGFP RPE + + + + Müller cell CRALBP + + − − Vimentin + + − − GFAP + + − − Photoreceptor Opsin Red/Green − + + + Opsin Blue − − + + Recoverin ND ND + ND Neuron in INL PKCα − − − − Ganglion Cell NeuN − ND ND ND Astrocytes GFAP − − − − +, indicates expression of GFP in a given cell type −, no GFP expression ND, Not Determined

Results:

-   -   All tested viral vectors were functional in the mouse retina.     -   scAAV8-pRLBP1(short)-eGFP vector leads to selective expression         of GFP in RPE and the Müller cells in the neural retina.     -   AAV8-pRLBP1(long)-eGFP leads to expression of GFP in RPE, Müller         cells and photoreceptors in the neural retina.     -   AAV8-pRPE65-eGFP and AAV8-pVMD2-eGFP lead to GFP expression in         RPE and photoreceptors in the neural retina.

CONCLUSION

These results demonstrate that the combination of promoter, AAV genome conformation and AAV capsid sequence can lead to different transduction properties in specific cell types, to achieve the desired effect. Expression of the RLBP1 gene product in RPE and Müller cells of the retina, represents the desired on-target cell type expression. RLBP1 short promoter packaged in a self-complementary genome in conjunction with an AAV8 serotype capsid induces gene expression in RPE and Müller cells in the neural retina without off-target cell expression.

The RLBP1-long promoter packaged in a single-stranded genome in conjunction with an AAV8 serotype capsid induces gene expression in RPE and Müller cells, which are on-target cell types, and also in photoreceptors, which is an off-target cell type.

The RPE65 and VMD2 promoter packaged in a single-stranded genome in conjunction with an AAV8 serotype capsid induces gene expression in RPE cells but also in photoreceptors, which is an off-target cell type.

Example 3 mRNA Based Assay to Measure Vector-Mediated Expression of a Human RLBP1 Transgene Relative to Endogenous Mouse RLBP1 mRNA Expression

The expression levels and tissue specificity of an rAAV-transduced transgene will vary depending on the vector serotype, the vector genome, the tissue-specific promoter used and the dose injected. A goal of gene replacement therapy is to achieve a level of expression that is sufficient to compensate for the missing endogenous gene expression while not over expressing the gene to toxic levels.

An assay has been developed to measure the vector-mediated expression of human RLBP1 mRNA relative to the endogenous levels of mouse RLBP1 mRNA following subretinal injections of various AAV vectors at different doses in wild-type mice. This assay utilized Taqman® Gene Expression Assays containing primers and probes for specifically detecting human or mouse RLBP1 cDNA. Prior to performing the experiment the Taqman® Gene Expression Assays were tested for species specificity using plasmid DNA containing either human or mouse RLBP1 cDNA sequences. In brief, Taqman® reagents were used to co-amplify either mouse or human RLBP1 cDNA with mouse GAPDH cDNA as an endogenous control. The levels of the mouse or human RLBP1 were normalized to the internal GAPDH control and then these normalized levels were compared with one another.

Supplies/reagents:

-   -   RNA extraction         -   Qiagen RNeasy micro kit (Qiagen cat #74004)         -   Qiagen RNase-Free DNase Set (Qiagen cat#79254)         -   Beta-Mercaptoethanol (Sigma cat#63689)         -   Qiagen Stainless-Steel 5 mm beads (Qiagen cat#69989)         -   2.0 ml Seal Rite Microcentrifuge tube (USA Scientific             cat#1620-2700)         -   Qiagen TissueLyser II (cat#85300)     -   cDNA Synthesis         -   High Capacity cDNA Reverse Transcription Kit (Applied             Biosystems cat#4368814)         -   RNase Inhibitor (Applied Biosystems cat#N8080119)         -   BioRad Thermal cycler     -   Relative Quantitation PCR         -   2× TaqMan® Universal PCR Master Mix (Applied Biosystems             cat#4304437)         -   20× TaqMan® Gene Expression Assay for human RLBP1 (Applied             Biosystems cat#4331182: Hs00165632.m1)         -   20× TaqMan® Gene Expression Assay for mouse RLBP1 (Applied             Biosystems cat#4331182: Mm00445129.m1)         -   20× Applied Biosystems® Mouse GAPD (GAPDH) Endogenous             Control (VIC®/MGB Probe, Primer Limited) (Applied Biosystems             cat#4352339E)         -   Applied Biosystems Real-Time PCR machine model 7900HT.     -   Test articles used in this example:         -   NVS8 viral vector         -   NVS10 viral vector         -   NVS4 viral vector         -   NVS2 viral vector         -   NVS6 viral vector

Protocol:

At the termination of the in vivo experiment neural retina was dissected out of the eyes, placed in a 2 ml microcentrifuge tube and flash frozen on dry ice. The remaining eye cup (minus retina and lens) was frozen in a separate tube. Samples were stored at −80° C. until RNA isolation. Total RNA was extracted using a Qiagen RNeasy micro kit with DNase treatment. For tissue homogenization and lysis, a Qiagen TissueLyzer was used. In particular, a 5 mm stainless-steel bead was added to each tissue-containing tube while on dry ice. Samples were transferred to room temperature and 350 μl of buffer RLT containing 1% beta-mercaptoethanol was added. Samples were processed on the TissueLyzer with a shaking frequency of 30 Hz for two 2 minute cycles. The standard Qiagen RNeasy micro kit protocol for RNA extraction with DNase treatment was then followed with one minor modification. Prior to elution the RNA column was allowed to air dry for >10 minutes to ensure elimination of residual ethanol. Total RNA was stored at −80° C. until ready for cDNA synthesis.

Total RNA concentration was determined using a Nanodrop spectrophotometer. Each sample was adjusted to a final concentration of 50 ng/μl. cDNA was generated using the Applied Biosystems High Capacity cDNA reverse transcriptase kit. A master mix of reagents from the High Capacity cDNA RT kit was prepared such that each 10 μl contained 2 μl of 10× High Capacity RT buffer, 0.8 μl of 25× dNTPs (100 mM), 2 μl of Reverse Transcriptase random primers, 0.4 μl of RNase inhibitor, 1 μl of Multiscribe Reverse transcriptase and 3.8 μl of RNAse-free water. 10 μl of the 50 ng/μl stock of each total RNA was dispensed into a well of a 96-well PCR amplification plate and then 10 μl of the RT master mix was added to each well. The plate was placed in a Bio-Rad thermal cycler and operated using the following parameters: 25° C. for 10 min, 37° C. for 120 min., 85° C. for 5 min then hold at 4 degrees until terminate program. cDNA was stored at −20° C. prior to Relative quantitative PCR reaction set-up.

The cDNA concentration was adjusted to a final concentration of 20 ng/μl by adding 5 μl of RNAse-free water to each well of the cDNA reaction (this is based on the initial total RNA concentration and assuming 100% conversion to cDNA). For each cDNA sample set up two different multiplex qPCR reactions; one using the mouse RLBP1 Taqman Expression Assay probes with the mouse GAPDH endogenous control, and the other using the human RLBP1 Taqman Expression Assay probes with the mouse GAPDH endogenous control. Each of these two reactions were performed in duplicate for each sample. For each sample, 5 μl of the 20 ng/μl cDNA sample was dispensed into a well of a 385-well plate. Two separate master mixes were prepared, one for the mouse RLBP1 Taqman assay and one for the human RLBP1 assay such that each 15 μl of mixture contained 10 μl of 2× TaqMan®Universal PCR Master Mix, 1 μl of 20× TaqMan® Gene Expression Assay for either mouse or human RLBP1, 1 μl of 20× Applied Biosystems® Mouse GAPD (GAPDH) Endogenous Control, and 3 μl of RNAse-free water. 15 μl of the appropriate master mix was dispensed into the well containing the cDNA. The plate was placed in an ABI 7900HT Real Time PCR machine and run using the relative quantitation program with the following parameters: an initial incubation at 50° C. for 2 min then 40 cycles of the following two steps, 15 sec. at 95° C. and 1 min. at 60° C.

The relative quantitation plate results were imported into a RQ study document using the ABI RQ Manager 1.2. The data were analyzed using the automatic threshold setting to generate average and average ΔCt which is the difference in Ct readings of the RLBP1 cDNA (mouse or human) minus the Ct of the internal endogenous GAPDH. The data were exported into Microsoft Excel and used to calculate the ΔΔCt value by subtracting the mouse RLBP1 ΔCt value from the human RLBP1 ΔCt for each sample. The relative expression was calculated using the calculation 2^(−ΔΔCt) this expresses the relative expression of human RLBP1 as a fold change of the mouse endogenous RLBP1 expression. To portray the results as expression of human RLBP1 as a percent of the mouse endogenous expression the relative expression value was multiplied by 100. Results: mRNA Expression.

FIG. 1A illustrates that NVS8, NVS4, NVS2 and NVS6 successfully transduce both the neural retina cells and the RPE cells in the posterior eyecup. Vector NVS10 transduces the RPE cells but barely at the level of detection limit in the neural retina.

FIG. 1B illustrates that NVS2 is the only vector to show mRNA expression in the neural retina at a lower dose of 1×10⁸ vg/eye.

CONCLUSION

These surprising results demonstrated that the specific combination of promoter, AAV genome conformation, and AAV capsid sequence can lead to different transduction properties in different cell types in the retina. In general, all tested vectors successfully lead to vector-mediated human RLBP1 mRNA expression. More specifically, NVS2 is the most potent vector in expressing human RLBP1 mRNA in the RPE cells (in the posterior eyecup) and in the neural retina in both doses tested (1×10⁹ and 1×10⁸ vg/eye), while NVS4 and NVS6 lead to detectable vector-mediated human RLBP1 mRNA expression at the dose of 1×10⁹ vg/eye, and only in the RPE at the dose of 1×10⁸ vg/eye. NVS8 and NVS10 lead to detectable mRNA expression in the RPE and neural retina at the dose of 1×10⁹ vg/eye but almost at the detection limit at the dose of 1×10⁸ vg/eye.

Example 4 Electroretinogram-Based Dark Adaptation Assay

One approach for assessing treatments that modify the visual cycle is to quantify the recovery of visual function in the dark following a bright light exposure (i.e. dark adaptation). Dark adaptation after extensive light exposure is driven largely by the ability of the eye to regenerate photopigment via the visual cycle. Modifications to the visual cycle achieved through treatment will therefore lead to a change in the kinetics of dark adaptation.

An assay has been developed to monitor the recovery of visual function in mice that is based on quantifying dark adaptation using an electroretinogram (ERG). The ERG-based assay typically proceeds over two days with an initial baseline and subsequent follow-up measurement to assess recovery after exposure to light that bleaches a fraction of the photopigment (photobleach). This procedure developed for testing the invention first determines the maximum electrical response of each eye 5 ms after a flash of light during the a-wave portion of the ERG trace. The test subsequently compares the 5 ms a-wave amplitude 4 hours after a photobleach to assess the fraction of maximum amplitude recovered in that time. If the visual cycle is functioning normally, the ERG amplitude will approach baseline values in 4 hours. A delayed visual cycle will result in lower recovery of photopigment with a corresponding reduction in ERG a-wave amplitude recovery after photobleach.

Supplies/Reagents:

-   -   ERG system: Diagnosys, Espion E2 console with ColorDome full         field ganzfeld stimulator     -   Ketamine     -   Xylazine     -   2.5% phenylephrine     -   1% cyclopentolate     -   0.5% proparacaine     -   Active electrode: Gold loop contact lens electrode (Mayo, part         number N30)     -   Reference electrode: Nasopharyngeal electrode (Grass, part         number F-ERG-G)     -   Ground electrode: Platinum needle electrode (Grass, part number         F-E2)     -   Hydrating drops: Novartis, Genteal Mild to Moderate     -   Syringe pump: Harvard Apparatus, part number Pump 11 Plus

Protocol:

Mice are placed in the dark overnight for approximately 20 hours before baseline ERGs are recorded. Immediately preceding recording, eyes are dilated with 1-2 drops of 1% cyclopentolate and 1-2 drops of 2.5% phenylephrine. 1-2 drops of 0.5% proparacaine (a topical anesthetic) are also applied. Mice are then anesthetized with an intraperitoneal injection of a cocktail of ketamine and xylazine (100-150 mg/kg and 5-10 mg/kg, respectively). Three electrodes are then placed to enable recording an ERG from one eye per mouse. The active electrode on the eye is a gold loop contact lens, the reference is a nasopharyngeal electrode placed in the mouth and the ground is a subdermal platinum needle electrode placed on the back just behind the head. Eyes are kept moist and electrical contact is maintained through continuous application of hydrating drops with a syringe pump (300 μl/hour). ERG amplitude is recorded by averaging the electrical response to three white flashes (2.7 log scotopic candela second per square meter) delivered by the xenon lamp in the ganzfeld dome. A-wave amplitude reported is the voltage measured 5 ms after the xenon flash as assessed using software analysis routines developed for this purpose (Mathworks, Matlab).

Dark adaptation is assessed by quantifying the ERG a-wave amplitude 4 hours after a photobleach. These experiments typically occur 48 hours after baseline determination. Mice are first housed in the dark overnight just as with the baseline measurements so that ERG recordings occur approximately 20 hours later. Eyes are dilated with 1-2 drops of 2.5% phenylephrine and 1-2 drops of 1% cyclopentolate immediately preceding photobleach. A sequence of 16 flashes of light (3.7 log scotopic candela second per square meter) is then delivered to the eye resulting in a photopigment bleach. Mice are placed back in the dark for 4 hours to recover visual function. ERGs are then recorded utilizing the same protocol used for the baseline determination. The recovery of visual function for each eye is defined as:

${DA} = \frac{a\text{-}{wave}\mspace{14mu} {amplitude}\mspace{14mu} 4\mspace{14mu} {hours}\mspace{14mu} {post}\text{-}{bleach}}{{baseline}\mspace{14mu} a\text{-}{wave}\mspace{14mu} {amplitude}}$

FIG. 2 illustrates the results of the assay when applied to RLBP1−/− and RLBP1+/+mice. RLBP1+/+mice exhibit nearly full recovery (up to 96%) 4 hours post-bleach. In contrast, RLBP1−/− mice recover minimal visual function (11%) at the same time point due to severely delayed visual cycle kinetics (Saari et al 2001). This 8-9 fold window between RLBP1+/+and −/− mice is the assay window achievable for testing vectors injected into RLBP1−/− mice.

Using the ERG-based dark adaptation assay described above, the improvement of dark adaptation efficiency is tested in RLBP1 knockout (KO) mice where therapeutic vectors are introduced subretinally. Since the subretinal injection involves the displacement of neural retina from the RPE, it is crucial to determine if the neural retina is reattached to the RPE to avoid false negative results for the test articles in the ERG assay. One week after subretinal injection of viral vectors into mouse eyes, optical coherence tomography (OCT) is performed to visualize the condition of the retina. Eyes with unresolved retinal detachment were excluded from ERG measurement.

At each time point, mice were dark adapted overnight (>12 hours) and the ERG a-wave amplitude from each eye was established as the maximum dark adapted response to light (100%). The fully dark adapted eyes were then exposed to a series of bright flashes (as described in previous section) and a-wave amplitude was quantified 4 hours later. The term “percentage of normal” is defined as the percentage of the second a-wave recovery measurement with respect to the value obtained from the maximum a-wave recovery measurement.

Positive efficacy, or efficacious effect, is defined as the difference between test measurement and negative (naïve) control being statistically significant at a given time point post-injection.

Test Articles Used in this Example Includes:

-   -   NVS1 viral vector     -   NVS2 viral vector     -   NVS3 viral vector     -   NVS4 viral vector     -   NVS5 viral vector     -   NVS11 viral vector

FIGS. 3A-D illustrate that viral vectors expressing RLBP1 improve the rate of dark adaptation in RLBP1 KO mice. Efficacy assessments were performed for each group vs. naïve controls with statistics calculated using a one way ANOVA with a Newman-Keuls multiple comparison test. The mean+3 standard deviations (SD) for naïve (uninjected) eyes and eyes receiving 1×10⁹ vg/eye of the negative control AAV-null vector (NVS11) for all related studies are shown to indicate the approximate threshold for efficacy (a-wave recoveries above this line typically exhibit statistically significant efficacy). This approach for displaying the degree of efficacy is similar to that presented in gene therapy publications (Jacobson et al. 2006 and Roman et al. 2007).

FIG. 3A shows that at a dose of 3×10⁸ vg/eye, NVS2 is efficacious in improving the rate of dark adaptation as early as 14 days post treatment, and the efficacy endures at least 350 days. A dose of 3×10⁸ vg/eye of NVS4 is also efficacious for at least 30-204 days post-treatment. NVS2 at the dose of approximately 3×10⁸ vg/eye has been tested in RLBP1 KO mouse model in 3 independent experiments. In each experiment at all time points tested up to 350 days post injection the vector demonstrated efficacy.

FIG. 3B shows that NVS1 at the same dose (3×10⁸ vg/eye) demonstrated efficacy starting 84 days post-injection, with efficacy enduring to at least 350 days. NVS5 and NVS3 at the same dose did not demonstrate efficacy for up to 154 days post drug administration. Data presented in FIGS. 3A and 3B suggested that even though the viral vector genome is equivalent, the vector can be of different potency when packaged in different AAV capsid serotype (NVS1 versus NVS2). In addition, the specific combination of vector serotype, promoter, and vector genome conformation can affect the potency of the vector (NVS1 carries a self-complementary genome while NVS3 and NVS4 carry a single-stranded genome, all with different promoter sequences). This result further confirms that the combination of genome conformation and capsid serotype can affect the efficiency of recovery outcome.

FIG. 3C shows that, at the dose of 1×10⁹ vg/eye, NVS2 is efficacious as early as 18 days post treatment, and the efficacy endures at least 375 days. At the dose of 1×10⁹ vg/eye, NVS11, which is a negative control AAV-null vector, did not show significant difference in improvement of rate of dark adaptation when compared to uninjected control (individual data points not shown, but the historical mean+3SD line is displayed for comparison). A dose of 1×10⁹ vg/eye of NVS4 is also efficacious for at least 30-204 days post-treatment.

FIG. 3D shows that at a dose of 3×10⁹ vg/eye, NVS3 and NVS5, respectively, are efficacious in improving the rate of dark adaptation as early as day 26 post-treatment, and the efficacy endures at least 371 days.

FIG. 4A demonstrates that NVS2 at multiple doses is efficacious at improving the rate of dark adaptation for at least 94 days post-injection. Both the 3×10⁸ and 1×10⁹ vg/eye groups were efficacious compared to naïve controls based on a one way ANOVA with a Newman-Keuls multiple comparison test. FIG. 4B displays the data from FIG. 4A in a different format. In this case, the plot displays the percentage of eyes/group with an a-wave recovery greater than that defined by the mean+3SD of the naïve group from several experiments. The results indicate that for NVS2, 50% of 3×10⁷ vg/eye treated eyes and 100% of 3×10⁸ and 1×10⁹ vg/eye treated eyes demonstrated efficacious a-wave recovery, and that a dose-response curve is established.

FIG. 5A demonstrates that NVS4 at multiple doses is efficacious at improving the rate of dark adaptation for at least 93 days post-injection. Both the 3×10⁸ and 1×10⁹ vg/eye groups were efficacious compared to naïve controls based on a one way ANOVA with a Newman-Keuls multiple comparison test. FIG. 5B displays the data from FIG. 5A in a different format. In this case, the plot displays the percentage of eyes/group with an a-wave recovery greater than that defined by the mean+3SD of the naïve group from several experiments. The results suggest that for NVS4, 85% of eyes treated with 3×10⁸ and 1×10⁹ vg/eye exhibited an increase in dark adaptation rate.

FIG. 6 demonstrates the increase in dark adaptation rate achieved with vector NVS2 generated by various production methods. NVS2 and NVS2a were both produced using two different CsCl gradient centrifugation methods while NVS2b was purified using column chromatography. Efficacy achieved 84 days post-injection with all three purification methods is indistinguishable based on a one way ANOVA with a Tukey's test. This result indicates that 3 independent productions of NVS2 in 2 independent laboratories yielded functional material resulting in similar efficacy in RLBP1 KO mice.

Summary of Example 4 Results:

-   -   Eyes injected with viral vector NVS2 exhibit an increased rate         of dark adaption at doses ranging from 3×10⁷ to 1×10⁹ vg/eye,         where efficacy lasts for at least 350 days post injection in the         RLBP1 KO mouse model.     -   Eyes injected with viral vector NVS4 exhibit an increased rate         of dark adaption at doses ranging from 3×10⁸ to 1×10⁹ vg/eye and         the efficacy endures at least 204 days at both doses.     -   Eyes injected with viral vector NVS1 exhibit an increased rate         of dark adaptation at the dose of 3×10⁸ vg/eye and the efficacy         endures at least 350 days.     -   Eyes injected with viral vector NVS3 and NVS5 exhibit an         increased rate of dark adaptation at the dose of 3×10⁹ vg/eye         and efficacy endures at least 371 days. Efficacy of NVS3 and         NVS5 was not observed at 3×10⁸ vg/eye for any time point tested.

Conclusion:

Viral vector NVS2 exhibits higher maximum recovery than equivalent doses of the other vectors tested. Additionally, the NVS2 vector-mediated efficacy appears to be indistinguishable when prepared using CsCl or column chromatography purification.

Summary of Results:

The results demonstrated that self-complementary AAV8-pRLBP1(short)-eGFP vector, the reporter gene surrogate version of the therapeutic vector NVS2, leads to RPE and Müller cell type specific expression with no detectable off-target expression, where the therapeutic vector NVS2 leads to at least 350 days of visual function recovery measured by a-wave recovery in RLBP1 mice at doses ranging from 3×10⁷ to 1×10⁹ vg/eye. This specific gene cassette when packaged in a single-stranded genome and packaged with the same serotype capsid 8 exhibits significantly lower level of gene expression in mice, as demonstrated by the measurement of mRNA expression level. The same self-complementary genome as NVS2 and packaged in AAV2 capsid, which is NVS1, demonstrated efficacious a-wave recovery (i.e.: an increased rate of dark adaption) at the dose of 3×10⁸ vg/eye for at least 350 days. This result suggests that NVS2 is a more potent viral vector than NVS1, which is likely due to the more efficient infection of AAV8 capsid than AAV2 capsid to the target cell types.

The results also demonstrated that AAV8-pRLBP1(long)-eGFP vector, the reporter gene surrogate version of the therapeutic vector NVS4, leads to RPE and Müller cell expression but also to photoreceptors. The therapeutic vector NVS4 leads to at least 204 days of efficacy at doses ranging from 3×10⁸ to 1×10⁹ vg/eye. The same genome in NVS4 but packaged in AAV 2 capsid, which is NVS3, leads to efficacious a-wave recovery at the dose of 3×10⁹ but not at lower dose tested (3×10⁸ vg/eye). The results demonstrated that AAV8-pRPE65-eGFP vector, the reporter gene surrogate version of the therapeutic vector NVS6, leads to RPE cell type expression with extensive photoreceptor off-target expression. When therapeutic vector NVS5, which carries the same genome as NVS6 but packaged into AAV2 capsid, is tested in RLBP1 KO mouse efficacy model, the results demonstrated that NVS5 endures positive a-wave recovery efficacy at the dose of 3×10⁹ vg/eye but not at lower dose tested (3×10⁸ vg/eye).

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1. A viral vector having a vector genome comprising a retinaldehyde binding protein 1 (RLBP1) coding sequence, wherein said vector is adapted to direct expression of an RLBP1 coding sequence in retinal pigment epithelial (RPE) cells and Müller cells of the retina.
 2. The viral vector of claim 1, wherein said vector comprises an adeno-associated virus (AAV) serotype 2 or 8 capsid.
 3. The viral vector of claim 2, said vector genome comprising in the 5′ to 3′ direction: (i) a 5′ ITR; (ii) a recombinant nucleotide sequence comprising an RLBP1 coding sequence; and (iii) a 3′ ITR.
 4. The viral vector of claim 3 where in the recombinant nucleotide sequence comprises in the 5′ to 3′ direction: (i) a promoter; (ii) an RLBP1 coding sequence; and (iii) an SV40 polyA sequence.
 5. The viral vector of 4, wherein the nucleotide sequence of said promoter is selected from SEQ ID NO: 3 and
 10. 6. The viral vector of claim 4 wherein the vector genome comprises in the 5′ to 3′ direction nucleic acid sequences selected from the group consisting of: a) SEQ ID NO: 2, 10, 5, 6, 8, and 9; b) SEQ ID NO: 2, 11, 5, 6, 8, 14, 9; c) SEQ ID NO: 2, 22, 5, 6, 8, 23, and 9; and d) SEQ ID NO: 2, 3, 4, 5, 6, 8, 23, and
 9. 7. The viral vector of claim 2, wherein said vector genome comprises in the 5′ to 3′ direction: (i) a 5′ ITR; (ii) a first recombinant nucleotide sequence; (iii) a non-resolvable ITR; (iv) a second recombinant nucleotide sequence; and (v) a 3′ ITR, wherein the first and second recombinant nucleotide sequences are self-complementary.
 8. The viral vector of claim 7 where in the second recombinant nucleotide sequence comprises in the 5′ to 3′ direction: (i) a promoter; (ii) an RLBP1 coding sequence; and (ii) an SV40 polyA sequence.
 9. The viral vector of 8, wherein the nucleotide sequence of said promoter comprises SEQ ID NO:
 3. 10. The viral vector of claim 8 wherein the vector genome comprises nucleic acid sequences in the 5′ to 3′ direction of: SEQ ID NO: 36, 62, 63, 64, 65, 66, 1, 3, 4, 5, 6, 8, and
 9. 11. A viral vector comprising a vector genome capable of expressing a heterologous gene in RPE cells and Müller cells of the retina, said vector comprising a) an AAV8 or AAV2 capsid and b) said vector genome comprising an RLBP1 promoter operably linked to the heterologous gene, wherein said RLBP1 promoter has a sequence selected from SEQ ID NOs: 3 and
 10. 12. The viral vector of claim 11, wherein the vector genome is self-complementary.
 13. A composition comprising the viral vector of any of the preceding claims.
 14. The composition of claim 13 further comprising a pharmaceutically acceptable excipient.
 15. A method of expressing a heterologous gene in retinal cells, the method comprising contacting said retinal cells with a viral vector comprising: a) an AAV2 or AAV8 capsid, and b) a vector genome comprising an RLBP1 promoter of SEQ ID NO: 3 or SEQ ID NO: 10 operably linked to the heterologous gene.
 16. The method of claim 15, wherein the retinal cells are RPE cells and Müller cells.
 17. The method of claim 16, wherein the vector genome is a self-complementary genome.
 18. The method of any of claims 15-17, wherein the heterologous gene is RLBP1.
 19. A nucleic acid comprising a gene cassette, said gene cassette comprises, in the 5′ to 3′ direction: (i) a 5′ ITR or a non-resolvable ITR; (ii) a recombinant nucleotide sequence comprising an RLBP1 coding sequence; and (iii) a 3′TR.
 20. The nucleic acid of claim 19 that is a plasmid.
 21. The nucleic acid of claim 19, wherein: (i) said 5′ ITR or said non-resolvable ITR have a nucleic acid sequence of SEQ ID NO: 2 or 1, respectively; (ii) said recombinant nucleic acid sequence comprises a promoter having a nucleic acid sequence selected from: SEQ ID NO: 3, 10, 11, 12 and 22 operably linked to said RLBP1 coding sequence having a nucleic acid sequence of SEQ ID NO: 3; or (ii) said 3′ ITR has a nucleic acid sequence of SEQ ID NO:
 9. 22. The nucleic acid of claim 19, wherein the gene cassette comprises a nucleic acid sequence selected from: SEQ ID NO: 51, 52, 53, 54, and
 55. 23. The nucleic acid of claim 19, further comprising the nucleic acid sequence selected from SEQ ID NO: 26, 27, 28, 29, 30 and
 50. 24. The nucleic acid of claim 19, wherein the gene cassette comprises, in the 5′ to 3′ direction, the sequences selected from: a) SEQ ID NO: 2, 10, 5, 6, 8, and 9, b) SEQ ID NO: 2, 11, 5, 6, 8, 14 and 9, c) SEQ ID NO: 2, 22, 5, 6, 8, 23 and 9, d) SEQ ID NO: 2, 3, 4, 5, 6, 8, 23 and 9, or e) SEQ ID NO: 1, 3, 4, 5, 6, 8, and
 9. 25. A method of treating a subject having RLBP1-associated retinal dystrophy, the method comprising administering to a subject the composition of claim
 13. 26. A method of improving the rate of dark adaption in a subject having RLBP1-associated retinal dystrophy, the method comprising administering to a subject the composition of claim
 13. 27. A method of expressing an RLBP1 coding sequence in RPE cells and Müller cells in the retina of a subject having RLBP1-associated retinal dystrophy, said method comprising the step of: contacting the retina of said subject with the viral vector of claim 6 or
 10. 28. The composition of claim 13 for use in treating a subject having RLBP1-associated retinal dystrophy.
 29. The composition of claim 13 for use in improving the rate of dark adaption in a subject having RLBP1-associated retinal dystrophy.
 30. The viral vector of claim 6 or 10 for use in expressing an RLBP1 coding sequence in RPE cells and Müller cells in the retina of a subject having RLBP1-associated retinal dystrophy. 